Isolated diaphragmatic hydatid cyst: a rare entity in the paediatric population

Isolated primary diaphragmatic hydatid disease (HD) occurs in approximately 1% of adult cases. However, this unique presentation of a pediatric diaphragmatic cystic mass has not been previously described in the literature. This study reports a rare case of a 12-year-old girl who was diagnosed with a diaphragmatic hydatid cyst. Surgical exploration via subcostal incision revealed an isolated cyst, free from the thoracic and abdominal viscera. Cystotomy, removal of daughter cysts, and excision of the pericyst cavity were performed, followed by diaphragmatic repair. Histopathological examination confirmed the diagnosis. The postoperative course was uneventful, and the patient completed an 8-week mebendazole regimen with no recurrence at 3 months' follow-up. This paper recommends including HD in the differential diagnosis for pediatric patients presenting with diaphragmatic lesions, particularly in regions endemic for echinococcosis.

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Publication Details

Journal
Journal of Surgical Case Reports
Published
2024-08-01
DOI
https://doi.org/10.1093/jscr/rjae488
Citations
2
Primary Topic
Parasitic infections in humans and animals
Type
article
Field-Weighted Citation Impact
0.85

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article

Isolated diaphragmatic hydatid cyst: a rare entity in the paediatric population

Amine Ksıa, Amani N. Alansari, S. Mani, Sabrine Ben Youssef et al.
2 citations
Journal of Surgical Case Reports
Parasitic infections in humans and animals
0.85
article

Isolated diaphragmatic hydatid cyst: a rare entity in the paediatric population

Amine Ksıa, Amani N. Alansari, S. Mani, Sabrine Ben Youssef, Raed M. Al‐Zoubi, Habib Ullah Joya
article en
2 citations

Abstract

Isolated primary diaphragmatic hydatid disease (HD) occurs in approximately 1% of adult cases. However, this unique presentation of a pediatric diaphragmatic cystic mass has not been previously described in the literature. This study reports a rare case of a 12-year-old girl who was diagnosed with a diaphragmatic hydatid cyst. Surgical exploration via subcostal incision revealed an isolated cyst, free from the thoracic and abdominal viscera. Cystotomy, removal of daughter cysts, and excision of the pericyst cavity were performed, followed by diaphragmatic repair. Histopathological examination confirmed the diagnosis. The postoperative course was uneventful, and the patient completed an 8-week mebendazole regimen with no recurrence at 3 months' follow-up. This paper recommends including HD in the differential diagnosis for pediatric patients presenting with diaphragmatic lesions, particularly in regions endemic for echinococcosis.

Journal of Surgical Case ReportsVol. 2024(8)
Qatar Airways (Qatar) (QA), University of Monastir (TN), Hospital Fatuma Bourguiba Monastir (TN), Hamad Medical Corporation (QA), Qatar University (QA)
Qatar National Library
Good health and well-being
Openalex Percentile: Top 26%
Parasitic infections in humans and animals
0.85
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Isolated diaphragmatic hydatid cyst: a rare entity in the paediatric population — Amine Ksıa, Amani N. Alansari, et al. · Journal of Surgical Case Reports (2024) | TGRS Research Map | TGRS