Evidence map›Paper›PMID 39559497›Full record

ArticleRadiology case reports2025

Right-sided Poland syndrome with no classical hand deformity: A case report.

Sharma Poudel, Amrit Bhusal, Aalok Kumar Yadav, Santoshi Yadav, Tek Nath Yogi

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In one paragraph

Article in Radiology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sharma PoudelDepartment of Radiology, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Amrit BhusalDepartment of Radio-Diagnostics and Imaging, BP Koirala Institute of Health Sciences (BPKIHS), Dharan, Nepal.
Aalok Kumar YadavDepartment of Radiology, Tribhuwan University Teaching Hospital, Kathmandu, Nepal.
Santoshi YadavDepartment of Pediatrics, Kanti Children's Hospital, Kathmandu, Nepal.
Tek Nath YogiBP Koirala Institute of Health Sciences (BPKIHS), Dharan, Nepal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poland syndrome (PS) is a rare congenital condition characterized by the developmental anomaly of the chest wall, and classically presents with ipsilateral agenesis/hypoplasia of sternocostal head of pectoralis major which remains as the essential feature of the condition. It may or may not be associated with ipsilateral limb abnormalities. Diagnosis is mainly clinical. Imaging modalities like chest X-Ray, CT chest, US, and 3D-VRT CT can be used to know about the extent of involvement of this anomaly. We hereby present a case of a 25-year-old male who visited our hospital with chief complaint of poor development of right-sided chest wall, who was later diagnosed with right-sided Poland syndrome with no classical hand deformity. Every physician must put a differential diagnosis of PS in the back of mind while dealing with the case of poor development of chest wall.

Indexed as

Case reportChest X-rayCT chestHypoplasiaPoland syndrome

Identifiers

PMID39559497
PMCPMC11570410

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