Clinical and Radiological Features in Poland Syndrome: Report of 3 Cases and Review of Literature

Autor: Fatima Chait MD, Nourrelhouda Bahlouli MD, Rachida Chehrastane MD, Nidal Mrani Alaoui PhD, Fadoua Boughaleb MD, El alami Zouheir PhD, El Medhi Tarik PhD, Nazik Allali PhD, Siham El Haddad PhD, Latifa Chat PhD
Jazyk: angličtina
Rok vydání: 2023
Předmět:
Zdroj: Global Pediatric Health, Vol 10 (2023)
Druh dokumentu: article
ISSN: 2333-794X
2333794X
DOI: 10.1177/2333794X231219388
Popis: Poland syndrome is indeed a rare congenital malformation that can present with various degrees of thoracic and homolateral upper limb anomalies. The classic features of Poland syndrome include agenesis or hypoplasia of the sternocostal head of the pectoralis major muscle, hypoplasia of the nipple, absence of subcutaneous fat, multiple rib abnormalities, and sometimes Sprengel deformity (elevation of the scapula). Additionally, ipsilateral symbrachydactyly (combination of “short fingers” with cutaneous syndactyly [fused fingers]) may also be observed. However, it’s important to note that not all of these findings are always present in every patient, and the combination of features can vary greatly. Surgical treatment for Poland syndrome primarily focuses on improving pulmonary functions resulting from severe thoracic deformities. However, it is frequently performed with the additional goal of enhancing cosmetic appearance. In recent times, the use of adipose-derived mesenchymal stem cells and fat transfer has shown promising results for correcting chest defects and breast augmentation. In our study, we present a series of 3 cases that were referred to our institution due to thoracic deformities associated with Poland syndrome.
Databáze: Directory of Open Access Journals