Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence)
Orphanet Journal of Rare Diseases volume 15, Article number: 201 (2020)
Poland syndrome (OMIM: 173800) is a disorder in which affected individuals are born with missing or underdeveloped muscles on one side of the body, resulting in abnormalities that can affect the chest, breast, shoulder, arm, and hand. The extent and severity of the abnormalities vary among affected individuals.
The aim of this work is to provide recommendations for the diagnosis and management of people affected by Poland syndrome based on evidence from literature and experience of health professionals from different medical backgrounds who have followed for several years affected subjects. The literature search was performed in the second half of 2019. Original papers, meta-analyses, reviews, books and guidelines were reviewed and final recommendations were reached by consensus.
Being Poland syndrome a rare syndrome most recommendations here presented are good clinical practice based on the consensus of the participant experts.
This project was undertaken on the behalf of the Italian Association of Poland Syndrome (AISP), a non-profit organization supporting clinical, social and scientific activities for the benefit of persons affected by Poland syndrome (PS), with the aim of providing best-practices recommendations for the management of affected individuals. This work is based on peer-reviewed scientific literature intermingled with the personal experience of the authors who are familiar with PS and come from different areas of expertise. The consensus was reached through a slightly modified Delphi process , which allows agreement based on guide practice when published evidence is lacking.
People living with PS usually face a diagnostic “odyssey” undergoing multiple radiological, clinical and genetic tests, which are not always suitable. Published materials and personal experiences were here discussed: the provided recommendations should be considered a consensus based on the opinion of clinical experts with years of experience on PS, as further levels of evidence are not always available in the literature. People with PS typically miss one pectoralis major muscle . In most affected individuals, underdevelopment selectively affects the sternocostal head of the affected pectoralis major muscle with consequent asymmetry of the chest. In some cases, additional omolateral muscles of the chest, shoulder and upper limb, may be missing or underdeveloped. Bones of the rib cage can be also affected with shortened/missing/supranumerary ribs and fused/malformed/supranumerary vertebrae, potentially leading to more severe thoracic deformations and respiratory distress. Mammary gland and nipple hypo/aplasia also occur along with sparse or ectopic omolateral axillary hair .
A subset of PS patients also have hand malformations affecting the same side and commonly including brachydactyly with or without syndactyly of the central fingers [4, 5]. Additional upper limb anomalies of PS include mild shortening of forearm bones and mild underdevelopment of the arm muscles; but these features are not easily detected unless accurate measurements are carried out. In the absence of bony involvement, musculoskeletal manifestations of PS usually have trivial or minor health implications and, therefore, can go unnoticed for years. By contrast, severely affected individuals with multiple muscle and bony abnormalities of the chest, upper limb or both are recognized at birth. In a minority of the cases, PS combines with extra-musculoskeletal congenital defects such as lung or kidney malformations and dextrocardia . Rarely, chest and/or upper limb abnormalities of the PS type occur bilaterally . Although bilaterality might be an underestimated feature of PS, the existence of a PS variant symmetrically affecting both sides of the thorax is still a matter of debate .
Etiology and pathogenesis of PS
To date, the etiology and pathogenesis of PS are still unknown. Most PS cases are sporadic. This evidence together with the striking asymmetry characterizing the typical patients are arguments against a mendelian etiology for PS. Nevertheless, a genetic etiology cannot be completely excluded due to the existence of familial cases, as well as the possibility of genetic mosaicism potentially explaining also the sporadic ones [9, 10]. Indeed, sporadic cases could be also explnained by the intervention of genetic and environmental factors according to a multifactorial poligenic model. Concerning the pathogenesis of PS, there are many available hypotheses in literature. The most commonly agreed one is that dysembryological process leading to PS is caused by a vascular defect of the subclavian artery (which nurtures the developing scapulo-humeral girdle region) around the 45th day of embryonic life. This causes an early insufficiency of inflow to the distal limb and to the breastplate, eventually leading to the main musculoskeletal features of PS. According to this model, the vascular insult might be secondary to a variety of environmental and constitutional factors which remain undefined . Alternatively, and considering PS as a polygenic trait, it may be due to the involvement of genes regulating embryonic development, in particular of pectoral girdle, whose variants could be transmitted to the patient from healthy parents and be at the origin of PS.
Consensus decision making to reach agreement among participants
A working group of 35 experts has been set up, including clinical and molecular geneticists, pediatricians, plastic, thoracic and hand surgeons, psychologists, radiologists and physical therapists, to formulate best practice recommendations for PS based on the consensus reached through the Delphi process, which has been recognized as a valid approach to ensure relative anonymity and economy. Three experts (MC, IB, LM and MT) have identified five main areas to be explored: 1) Diagnosis, 2) Surgical treatments and specific medical approaches on the major symptoms, 3) Plastic surgery and rehabilitation, 4) Psychological issues and social assistance, 5) Clinical follow-up and general management. Each participant was asked to provide provisional recommendations (N = 103) based on their personal experience and bibliographic knowledge: the PubMed/MEDLINE electronic databases were searched for suitable articles from 1990 to 2019. All PS synonyms were searched in MeSH terms, title and abstract. Subsequently, the panel members independently evaluated the initial recommendations proposed regarding the topics listed above in an online survey (100% response rate): the participants were asked in two subsequent rounds of surveys whether they agreed, disagreed (they were also asked to provide a reason) or were unable to comment on any of them. The findings resulted in three possible grade levels: i) certainly useful/strong literature, ii) possibly useful/modest literature, or iii) Good Clinical Practice (GCP) but no relevant literature available. The recommendations were accepted if ≥50% of the experts agreed. For the last step, the recommendations approved by the previous surveys were discussed in a face-to-face consensus meeting held on October 2019 and hosted in the Policlinico Hospital in Modena (number of experts participating: 21). Disagreements were resolved through discussion or asking for the opinion of a third expert. Although consensus was reached, comments were considered to better clarify the recommendations. An expert without the right to vote (MC) facilitated the entire process.
Unilateral agenesis or hypoplasia of the (sternocostal head of the) pectoralis major muscle is currently considered pathognomonic of PS (Table 1) that is still exclusively a clinical diagnosis (for the additional features, refer to the Principal diagnostic criteria section).
The clinical diagnosis of PS may be suspected in neonatal/pediatric age in front of patients who present i) asymmetric hypoplasia of the pectoral muscles and any abnormalities of the thoracic cage, or ii) anomalies affecting the pectoral muscles unilaterally. Patients are rarely reported with bilateral pectoralis major muscle agenesis/hypoplasia. In adulthood, patients with unexplained muscle hypoplasia may be diagnosed with PS, especially if associated with asymmetric of the thoracic cage, anomalies of the mammary region (hypoplasia or agenesis of the breast and of the unilateral nipple) and abnormalities of the hand.
Since a gene(s) responsible for PS has not yet been identified, the diagnosis of PS is clinical and based on the recognition of the characteristic recurrent pattern of features along with an appropriate differential diagnosis. Agenesis or hypoplasia of the pectoralis major muscle is currently the cardinal feature mandatory for the diagnosis (Table 2). The pectoral muscle anomaly is generally easily observed by asking the patient to push the palms of the hands against each other with the arms positioned in front of the body . Additional commonly reported features include:
Absence or hypoplasia of other chest muscles: small pectoral muscle, anterior tightened muscle, gran dorsal muscle, deltoid muscle
Anomalies of the thoracic cage: agenesis or hypoplasia of one or more costal segments, pectus carinatum, excavatum, clavicular hypoplasia, pulmonary herniation
Abnormalities of the mammary region: agenesis or hypoplasia of the breast, areola and nipple
Abnormalities of the upper limb and shoulder
Absence or asymmetric reduction of axillary hairs
Other associated skeletal anomalies: Sprengel anomaly (congenital elevation of the scapula secondary to absence of the upper portion of the serratus anterior muscle), radioulnar synostosis, emivertebre, vertebral fusions.
They are also described as associated malformations:
hepatic and/or biliary tract malformations.
Ultrasound (US) represents the first line diagnostic imaging method to support or confirm the clinical diagnosis of PS, due to its easy accessibility, cost-effective and radiation free modality. An accurate description of soft tissue and chest wall morphological abnormalities, not always easy to identify during clinical assessment, is of outstanding importance since to different types of malformation correspond a different therapeutic approach. Evaluation by US is therefore recommended (Table 3) to assess pectoralis muscle (major and minor), breast characteristics of the two halves of the thorax, and could be used as screening exam for cardiac and renal abnormalities . Associated rib abnormalities are detectable by US but, when suspected, imaging work-up should be completed with other diagnostic modalities described later. In case of specific clinical concern, by means of US performed by radiologists with expertise in musculoskeletal pathology, is possible to examine complex dysmorphism of distal upper extremities: i.e. mapping of hand muscle could address surgery and rehabilitation, moreover in pediatric patient less suitable for MRI scanning.
US examination should be performed with an high frequency probe, with a musculoskeletal preset, and should be bilateral and comparative, detecting all the 3 heads of the pectoralis major muscle (clavicular, sternocostal and abdominal) with sagittal and transverse scans, the pectoralis minor muscle and the mammary gland. Thereby US allows to classify different pectoralis major abnormalities into three morphologic groups: i, total agenesis of the muscle; ii, agenesis of the sterno-costal part with normal clavicular component; iii, partial agenesis of the sterno-costal part with normal costoclavicular component. Moreover US is able to recognize regional anomalies affecting the pectoralis minor and regional vessels . For evaluation of pectoralis major and minor muscle, this “4 view” standard assessment is proposed (Table 4, Figs. 1,2, 3, and 4). In Prenatal setting, US screening is strongly limited by the difficulties in appreciating such a thoracic asymmetry. Only severe bone manifestations involving hands or rib cage might be identified on occasion of US morphological examination, but fetal movements often reduce the detection rate especially in low-risk pregnancies. Any prenatal findings is aspecific and need to be confirmed with clinical examination after birth . On the basis of the current state of knowledge no further radiological analysis are indicated in uterus if parents are affected by the syndrome. A complete radiological workup as well as US of the pectoralis region, echocardiography and abdominal ultrasound, inckudes also X ray of the thorax if rib cage abnormalities are clinically suspected . In selected case of severe chest malformation, thoracic CT and /or MRI are appropriate for a thorough pre-surgical assessment. In particular CT scan with contrast may provide a more detailed depiction of bone anomalies and vascular relationships. Only in few selected patients should be considered a complete radiologic study of the skeletal and muscles of hands, forearms, upper arms and/or scapula with X-rays or CT (other than MRI) in order to better detect complex anomalies clinically evident and define a pre-surgical planning [17, 18]. Wide consensus is reached among experts about the “second line” role of CT and MRI in PS diagnostic-therapeutic process. Both CT and MRI clearly depict the absence of the pectoralis major muscle and allows better appreciations of other nearby associated musculoskeletal and inner organs anomalies but, considering radiation exposure of CT, necessity for anesthesia in younger pediatric patient who undergoes MRI other than lower cost-effectiveness, should not be indicated as first approach. In setting of pre-surgical planning, MRI can provide the most of necessary information without exposing patient, often in young age, to the risk of radiations. Regarding thoracic MRI, in order to obtain a highly defined picture of a structure in constant movement (breathing related), specific sequences and adjustments are required.
Literature is scanty on the differential diagnosis of PS. Until the preparation of this manuscript, 33 papers appeared in PubMed under the research strings [“Poland syndrome” AND “differential diagnosis”] and [“Poland sequence” AND “differential diagnosis”], or [“Poland’s syndrome” AND “differential diagnosis”] and [“Poland’s sequence” AND “differential diagnosis”]; but, among them, differential diagnosis of PS was discussed only in four of them [19,20,21,22]. Of these papers, two were dedicated to the radiological differential diagnosis of unilateral hyperlucent lung at standard radiographs [20, 21], one is a systematic review on controversies in PS , and the remaining is a case report pointing out a possible overlap between PS and localized (thoracic) lipoatrophy . Accordingly, a satisfactory differential diagnosis of PS is carried out by the intersection of practitioner’s experience on human malformation patterns and the “complexity” of the presenting phenotype. Scenarios of differential diagnosis of PS include:
Unilateral PS without additional skeletal/limb anomalies;
Unilateral PS with additional skeletal/limb anomalies;
PS “plus” (i.e. PS with additional anomalies not regularly considered part of the PS phenotypic spectrum);
Unilateral hyperlucent lung at thoracic X-rays.
The diagnosis of PS is usually clear-cut in the “typical” patient presenting with isolated unilateral hypo/aplasia of the major pectoris muscle with or without hypo/aplasia of the overlaying mammary gland/areola/nipple (Table 5). The most common differential diagnoses include thoracic asymmetry due to clinically significant thoracic scoliosis and/or anomalies of the bony structures (sternum, ribs, vertebrae), isolated congenital mammary gland/areola/nipple asymmetry (particularly, in women) or unilateral hypo/aplasia, and consequences of thoracic traumas/surgery. Additional disorders that may present cause localized hypo/atrophy of the thoracic soft tissues include localized lipoatrophy , morphea or localized scleroderma, Becker nevus syndrome and Parry-Romberg syndrome (extending to the thoracic soft tissues). Finally, thoracic asymmetry might be also the result of unilateral diaphragmatic acquired or congenital abnormalities. Physical examination accurately assessing the soft tissues of the thoracic cage in combination with scrutiny of the past medical history and, in selected cases, radiological investigations support the practitioner in the differential diagnosis. In patients presenting with (usually) unilateral or asymmetric upper limb involvement, the identification of the concurrent omolateral pectoralis anomaly, which is considered necessary and pathognomonic of PS, separates patients with PS from those with partially overlapping upper limb malformations. Considering the pattern of upper limb involvement in PS, the most common differential diagnosis is ectrodactyly, which defines a developmental deficiency of the distal central rays of the limb resulting in hypo/aplasia of the central digits extending, in some patients, to the corresponding metapods. The typical presentation of hand ectrodactyly is a two- or three-finger hand with a cleft extending up to the carpal bones. Less frequently, the typical brachysyndactyly observed in PS might be confused with the more common transverse terminal limb deficiencies. In these cases, differential diagnosis is usually resolved at physical examination of the thoracic cage. Patients with bilateral PS are rare in clinical practice, although some authors speculated that, in PS, bilateral features should not surprise and could be underestimated in the current literature . In PS, bilateral presentation rises additional, though exceptional differential diagnoses mainly in the field of skeletal dysplasias leading to thoracic cage hypoplasia. Accordingly, one case with “bilateral” PS has been published, which has been subsequently reassigned to the diagnosis of “thoracic dysplasia” [23, 24]. In this scenario, physical examination by an expert in human malformation patterns and total-body skeletal radiograph allows differential diagnosis. Exceptionally, PS presents in combination with additional anomalies, which are nosologically separated from PS. Sprengel deformity (i.e. hypoplasia, and upper and medial dislocation of the scapula) has been recently recognized as the most common accompanying feature of PS . PS can also associate with other (usually) sporadic malformation patterns (with unknown or heterogeneous etiology) affecting the cephalic pole and/or the upper segments of the musculoskeletal system. In particular, PS combines recurrently with Moebius syndrome in the literature and this phenotype has been defined Poland-Moebius syndrome . In single reports, PS concurs with Adams-Oliver syndrome , Klippel-Feil syndrome , facio-auriculo-vertebral dysplasia , and frontonasal dysplasia . Carey-Fineman-Ziter syndrome is an ultrarare congenital myopathy with marked facial weakness and additional features, also including PS . Carey-Fineman-Ziter syndrome is easily differentiated from the “simpler” PS by the unique pattern of presenting features. It has been recently associated with recessive variants in MYMK . Unilateral agenesis of the major pectoris muscle (with or without hypoaplasia of the overlaying mammary gland/areola/nipple) generates a difference in radiolucency of the lungs at standard X-rays. Such a radiological presentation is in common with a wide variety of acquired disorders and congenital conditions, whose extent is much beyond the scope of these recommendations. It is relevant, however, to note that, in addition to PS, many different pleural, lung parenchymal, pulmonary vasculature, central airways and mediastinal anomalies, as well as technical issues (e.g. patient rotation and lateral decentering) may cause unilateral hyperlucency of the lungs at standard X-rays [20, 21].
Communicating the diagnosis
The diagnosis of PS is arrived at in most cases within the first year of life . It is often communicated to parents who are unaware of the presence of the disorder . As for any newborn with congenital anomalies the diagnostic pathway and process should be communicated to the parents by explaining that the waiting time is necessary to receive the results of all requested investigations for an accurate evaluation (Table 6). The diagnosis should be addressed to both parents, since they are the “care coordinator”, a role that should be filled formally by a provider of the healthcare system . The information should be delivered gradually and adapted to the family’s socio-cultural level. Once the medical team is confident in the diagnosis of PS, it is important to underline that PS is not progressive and that, in the absence of severe rib cage malformations, its survival rate is comparable with the general population. A normal psychomotor development is expected and the malformation does not affect the growth. Correct education allows the development of manual skills even in the carriers of severe malformations. The communication of the diagnosis should occur in the presence of a psychologist or if this is not possible, an external psychological help should be suggested to support families and patients in coping with the disease. The continuity of care must be guaranteed and, if the specialist surgeon is not available in the clinical team, the contacts of the most appropriate specialist (s) for surgery must be given to the patients/families during the diagnosis and the follow-up. They should be also informed about parent/patient organizations  such as AISP. A minority of cases is diagnosed in adolescence or adulthood. Dissatisfaction with body shape can be a source of distress that may significantly affect the dimension of one’s health. Puberty, in particular, is characterized by many sometimes dramatic physical, physiologic, biochemical and personality changes that occur when teens are particularly sensitive to the opinions of others .
Most cases are sporadic, affected children of unaffected parents with no family history of congenital anomalies. Rare familial cases are reported in literature with a rate ranging from 4.2% (PS families with recurrence of pectoral muscle defects) to 8.4% (Poland-like syndrome families with PS index case and ≥ 1 relative(s) showing normal pectoral muscles but with upper limb and/or thoracic anomalies common in PS) . In the presence of sporadic cases the risk of recurrence, i.e. the risk that the same couple has a second affected child, is low. For familial cases, the recurrence risk is higher than that of the general population and must be calculated in accordance to the possible inheritance pattern (Table 7). It is therefore of fundamental importance to clinically evaluate the parents of affected children to exclude they could present mild, underdiagnosed forms that could therefore turn an apparently sporadic case into a familial case thus increasing the risk of recurrence. Genetic counseling is essential in all cases of PS and should be focused on informing patients that:
the pathogenic mechanisms underlying PS are still unknown;
most PS patients present in isolated form;
most cases of PS are sporadic but about less than 10% show familial recurrence, with higher prevalence in males, which suggests a genetic, hereditary basis;
to date, different models of transmission have been hypothesized, including autosomal recessive (recurrence risk of 25%) and autosomal dominant with incomplete penetrance (up to a 50% risk of recurrence);
sporadic cases can be explained by the appearance of de novo mutations;
Surgical treatments and specific medical therapies on the major symptoms
There is not any definitive solution to treat PS as well as any other genetically determined malformation syndrome. However, a surgical treatment of the major abnormalities and medical complications are appropriate and do not differ from that of other similar isolated malformations in the general population.
In the literature, there are no strict guidelines or indications regarding thoracic surgery in PS (Table 8). In the experience of the group of pediatric and thoracic surgeons who are the authors of the present recommendations, thoracic surgery is not always necessary in PS . The indication to thoracic surgery are usually related to severe rib cage anomalies, either regarding anterior chest wall (pectus excavatum, carinatum or combination of both) or ribs (rib agenesis). In case of anterior chest wall defect, the indication to the surgery can be cosmetical or functional. If the heart or the lungs are compressed by a pectus excavatum, a retrosternal metallic bar (Nuss procedure) is helpful to lift the sternum up and releiving the visceral compression. In case of asymmetric anterior chest wall without heart/lung compression, cosmesis can be improved with cartilage resection or osteotomy or both. In young patients, with a compliant chest wall, conservative treatments as FMF brace or vacuum bell can be used. In case of rib agenesis, surgery aims to give more protection to the thoracic organs, although no reports of traumatic complications have been reported in PS patients to the best of our knowledge. Thoracoplasty for rib agenesis is performed also to abolish paradoxycal respiration and stabilize the lungs and rib cage during forced inspiration/exhalation cycle. In order to obtain the stabilization of rib cage, different surgical solutions can be chosen, mainly using non absorbable prosthetic mesh or metallic prosthesis. Goretex mesh can be used successfully especially if the rib defect is not too wide, usually in case of absence of one or two ribs. If the defect involves three or more ribs, it is better to reinforce the rib cage by using a metallic prosthesis. In recent years, 3D printed metallic prostheses have been successfully implanted in PS patients. Goretex mesh is usually used above the metallic prosthesis to avoid skin erosion. It is usually better to correct a severe chest wall anomaly (if present) before breast/pectoral reconstruction, to improve the final result. In some cases, chest wall anomaly can be corrected at the same time of plastic surgery first step. The combined approach has the advantage of optimizing skin incision, reducing the surgical procedures, the number of hospitalizations and the dyscomfort for the patient. Regarding the best age for surgery, it is usually not necessary to operate the patients before 12-13 years of age. Ideally, thoracic reconstruction around 14-15 years of age when the thoracic growth is already advanced is our preferred time.
Hand anomalies in PS can show many forms of clinical presentation varying from a hypoplasic but functional hand to severe grade of symbrachydactyly with one or more absent fingers (Table 9). Moreover, there are a group of patients which are not affected by hand malformation, presenting the only absence of pectoral muscles. Clinical examination should not be limited to the hand but the entire upper limb must be checked because of the chance of malformations affecting the wrist, the elbow and the shoulder. Classifying the anomalies of the hand represents an important step which has a direct correlation with the choice of treatment; many classifications have been proposed but the majority were focused exclusively on the hand missing the likelihood of an involvement of other district of the upper limb. In 2012, a new system has been published and it can be considered more useful because it takes into consideration the entire upper limb . Eight types of clinical aspects have been considered:
Absence of hand/upper limb anomalies
Hypoplastic hand without morphologic and functional anomalies
Symbrachydactyly with 5 functional fingers and possible morphologic anomalies of the phalanges and partial range of motion
Symbrachydactyly with some functional fingers
Symbrachydactyly with absent or nonfunctioning fingers
Classic hand anomalies of PS with proximal radioulnar synostosis
Classic hand anomalies of PS with congenital high scapula
Other associated anomalies
Reconstructive planning should be discussed with the parents, adapting it to the type of deformity.
Children with normal hand (type I) or with hypoplasic but functional hand (type II) do not need any surgical treatment which is necessary instead for type III and in particular for types IV and V in order the improve hand function.
The issues the surgeon must deal with are the presence of syndactyly and the absence of phalanges (typically the middle phalanx) or entire fingers. Timing of surgery depends on the type of malformation. The correction of syndactyly should begin between 12 and 24 months of life, however, in case of syndactyly between finger of disparate length, early surgery is recommend between 6 and 12 months in order to reduce the risk of flexion contracture or angular deformities . The reconstruction of the second and third web spaces can be delayed until 18 months of age without adverse effect on hand function development. Surgical techniques do not differ from those adopted in other forms of syndactyly by means of local flaps (VY – Double Z – Z plasty at four tatters) to reconstruction the web space as well as the digital surfaces. Surgeons may need to use a skin graft for the uncovered areas; the volar surface of the wrist or the groin are the most common donor site. However, the use of hyaluronic acid scaffold for skin regeneration in syndactyly release surgery may be take into consideration as an alternative to the use of skin graft, due to the good results reported in young patients . After surgery an occlusive bandage should be applied and the first wound care is recommended after 2 or 3 weeks.
However, some patient may need an early dressing in case of infection, exudate or insufficient care of the dressing by the parents. In case of symbrachydactyly with phalanx absence, two options may be proposed to the parents, according to the grade of malformation: i) Non microvascular free phalangeal transfer from the foot, or 22) Microvascular digital transfer from the foot.
The first option should be proposed in case of symbrachydactyly with the presence of the proximal phalanx in order to increase the length of the single ray. Conversely, microvascular transfer is the only option in case of a peromelic hand or in the rare situation of a congenital metacarpal amputation. However, parents are often frightened from the idea of using the foot as donor site as well as from the risk of failure of a microsurgical transfer whereas they usually accept better the proposal of a free phalangeal transfer also considering the lesser functional and aesthetic result.
Finally, physicians must follow the patient until the end of skeletal of skeletal growth, because recurrence of syndactyly, secondary to scar hypertrophy, may be possible. When a recurrence occurs, it should be corrected, when possible, during adolescence in order to reach a definitive result.
Reconstructive surgery in PS has a mainly aesthetic meaning and it aims to improve quality of life (Table 10). The asymmetry involving the breasts, in fact, is often moderate or severe and it is made even more complex by the underlying thoracic malformations. Social aspects in case of bodily malformation cannot be ignored, both for male and female patients. A single defect, in fact, can affect the overall physical appearance up to create a variable degree of uneasiness in social relations . Patients affected by PS seem to experience high level of body uneasiness during adolescence . The reconstructive path, for this reason, can start during puberty and it depends strictly on the characteristics of the mammary / thoracic malformation, on the anatomical characteristics of the patient and on the psychological condition linked to the malformation. First of all it is important to classify the malformation: TNB classification is the most recent specific classification of thoracic, breast and nipple malformations which guides the surgeon in choosing the surgical path [40, 44]. A customized approach is therefore necessary even in relation to patient’s age, expectations and needs . Patients suffering of PS can contact the surgeon at any age depending on the time of diagnosis. Specialist interviews in the neonatal period and/or before puberty are only intended to reassure caregivers. Reconstructive plan can benefit from the modern breast reconstructive surgery techniques and should be the least invasive and debilitating for the patient given the main aesthetic purpose of the reconstruction and the musculoskeletal malformative characteristics that often affect the chest. Muscle transpositions should be used in selected cases after an accurate evaluation of the pros and cons of the procedure based on the anatomical characteristics (back, shoulder, posture, …) and life habits (sport activity, work activity, hobbies, …) of the patient. Muscle transpositions shouldn’t be used in non-adult patients, or even in patients who have not fully completed their psycho-physical development and who have not clearly outlined their social and working life habits . Reconstructive surgery can help especially younger patients (teenagers) to experience the aesthetic stigmata of the disease less traumatically, accompanying them on a path of growth and positive development of their body image. Soft tissue reconstructive surgery cannot be definitive; breast, muscles and adipose tissue involved in the malformative feature are tissues in continuous evolution based on age, physiological changes (pregnancy) and life habits and, for this reason, it may be necessary to rework them over time to maintain the desired aesthetic result.
The rehabilitation plan must be scheduled after each intervention on the basis of illness-specific criteria and specific surgical procedures (Table 11).
Psychological issues and social assistance
Currently, there is no scientific literature on psychological support for patients, and their families, suffering from PS (Table 12). In contrast, clinical practice highlights the importance of psychological support for the patient and his family. Furthermore, the psychologist appears to be an important resource also within the multidisciplinary specialist team both for drafting the protocols for taking charge  and for supporting colleagues during the various stages of the diagnostic, care and assistance process . Since the syndrome is increasingly diagnosed at birth, psychological support must first be directed to parents to elaborate painful experiences that could affect the attachment and care of the child and thus reinforce parenting skills. Subsequently, as the child reaches more and more autonomy, the support is necessary both for the parents and for the subject himself to avoid developing feelings of inadequacy and consequent socialization problems. About the choice to undergo surgery, especially in adolescence, it is useful that the decision is reached with the help of the psychologist, after assessing the subject’s psychological conditions, in full awareness and self-determination so that the result is satisfactory . It is not recommended to take the intervention exclusively on the advice of medical specialists. When the diagnosis is late, in adolescent or adult age, the psychodiagnostic evaluation is strongly recommended to check how the anomalies caused by the syndrome have affected the subject’s life , self-image and relationships with others . The request for correction of anomalies must be carefully considered and examined in depth to exclude unrealistic and unrealizable expectations .
Clinical follow-up and general management
Following the diagnostic classification, people affected with PS are followed by periodic follow-up visits to manage the main complications of the disease, such as functional and aesthetic issues (abnormalities of limbs, paroxysmal movements of the chest wall, reduced lung function, muscle weakness, scoliosis). Pediatric and plastic surgery examination for thoracic abnormalities (ribs, condrosternal cartilages, pectoral muscles, mammary gland) involves periodic clinical examinations and surgical correction in the most complex cases (Table 13).
The orthopedic evaluation and the hand surgery visit are indicated for the management of postural and upper limb anomalies, with a focus in the hand function. Periodical follow-up and physiotherapy in the most complex cases are also recommended (Table 14). Since in (rare) PS cases are also described for the presence of genitourinary (renal agenesis, renal ectopia, vesico-ureteral reflux and cryptorchidism) and cardiac (dextrocardia and inter-atrial defect) malformations it is advised to perform relevant specialist assessments when appropriate. Regarding risks and potential complications such as breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) in case of breast reconstruction with textured breast implant device, periodic clinical examination is recommended, as one would do to screen for implant complications such as capsular contracture.
The development of best standards of care and commonly approved procedures is urgently needed for all rare diseases (www.rarebestpractices.eu). In fact, to advance knowledge of PS the primary goal is defining evidence-based guidelines for those affected and their caregivers (Table 15). The present working group has formulated a total of 91 recommendations for the diagnosis and management of PS, based on a systematic review of literature and a consensus procedure. In total, 69 recommendations within 14 general principles, ranging from diagnosis to therapeutic approaches have been accepted with > 90% agreement among experts. When summarizing the degree of evidences available for the recommendations proposed in this review, some are “Good Clinical Practice” based on clinical experience of the authors. Key topics include assessment of the rib cage and other associated skeletal anomalies or abnormalities. Careful monitoring of the status and well-being of patients by an experienced multidisciplinary team and validated scores for the progression and follow-up are required in order to perform a structured assessment of the outcomes, as are long-term follow-up studies to clarify the risks of complications of therapeutic approaches. Given the rarity of PS, international collaboration is essential to provide specific support even in geographic areas lacking expert specialists.
To conclude, this initiative is based on the personal opinion of experts based on the best available evidence and provides recommendations for the options of diagnosis and treatment of PS patients, in order to improve the outcome for those affected. It will now be important to extend the discussion and the acceptability of our recommendations to a wider community of clinicians and families: a large international meeting on PS is expected to be scheduled in 2021 under the direct management of the AISP. In fact, one of the main purposes of the AISP is to improve the care and follow-up of people living with PS. For this reason the AISP has recently developed, in close collaboration with some clinical centers for the treatment of PS in Italy, the first registry for PS available in the world. The registry of PS is a tool for the systematic collection of personal and phenotypic data of affected people. Through the digitalization of high-quality clinical data, the registry aims to improve knowledge of PS and maximize natural history and epidemiologic studies.
The point of view of patients and caregivers
Purpose of AISP has always been to enhance the network of specialists and medical facilities who collaborates each other in order to allow the best possible care for patients on the Italian territory. Thanks to the drafting of this document, AISP did one important step closer to reach this aim and hope to provide clinicians and patients diagnostic and therapeutic approaches in PS as uniform as possible. AISP will surely advertise this report on its website and its social channels. This document will be shared with other European associations of PS patients and rare disease associations in Italy and in Europe and with the ERN of rare diseases. With the help of the clinicians involved in the draft, the document will be distributed to scientific society, medical structures, general practitioners and pediatricians, asking them to collaborate in its sharing. Moreover an informative brochure will be produced in order to enable patients to fully understand the document. The update of these recommendations will be promoted by AISP as part of its constant scientific activity and will be an integral part of the scientific program of AISP National Conferences.
Availability of data and materials
Data sharing not applicable as no datasets were generated during the current study.
Associazione Italiana Sindrome di Poland
Good Clinical Practice
Freire Martinez Ferro
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The authors are grateful to families for their cooperation and are also indebted to Ms. Clare Groarke for revising the manuscript. This work has been promoted within the European Reference Network on Rare Bone Disorders (ERN-BOND).
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Baldelli, I., Baccarani, A., Barone, C. et al. Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence). Orphanet J Rare Dis 15, 201 (2020). https://doi.org/10.1186/s13023-020-01481-x