Article: Rare scrotal chylous effusion: A case report.
SAGE open medical case reports
2024 Volume 12, Page(s) 2050313X241231368
Abstract: Klippel-Trenaunay syndrome is a rare congenital malformation predominantly affecting lower limb. In most cases, it is characterized by a classic triad of cutaneous capillary malformation (port-wine stain), lymphatic and venous abnormalities, in ... ...
Abstract | Klippel-Trenaunay syndrome is a rare congenital malformation predominantly affecting lower limb. In most cases, it is characterized by a classic triad of cutaneous capillary malformation (port-wine stain), lymphatic and venous abnormalities, in association with variable soft tissue and bone overgrowths. We describe a 48-year-old male presenting on the genitalia several whitish vesicles discharging a milky fluid compatible with chyle. Extensive radiology workup revealed pelvic megalymphatic malformations. Pelvic lymphatic ligations and bleomycin sclerotherapy only allowed a partial improvement. Given the high potential of recurrence, the patient will soon undergo a genetic evaluation for PIK3CA gene mutation and may need further systemic treatment with Sirolimus. As this scrotal chylous effusion in the setting of Klippel-Trenaunay syndrome is rare and highly affects the quality of life, we wanted to raise awareness of this entity and its management. |
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Language | English |
Publishing date | 2024-02-08 |
Publishing country | England |
Document type | Case Reports |
ZDB-ID | 2736953-5 |
ISSN | 2050-313X |
ISSN | 2050-313X |
DOI | 10.1177/2050313X241231368 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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