Results 71 to 80 of about 4,369 (185)
, 2021 Renal lymphangiomatosis is an unusual disorder. It may develop due to the abnormality of the intrarenal, peripelvic and perirenal lymphatics. The differential diagnosis contains renal lymphoma, polycystic kidney disease, multicystic dysplasia and renal ...
ERDEM, YUNUS +4 more
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Dermatologic Therapy, Volume 2026, Issue 1, 2026.Background Cutaneous metastases are uncommon but clinically significant manifestations of internal malignancies and may indicate advanced disease or, in certain cases, represent the initial sign of cancer. Their variable clinical and histopathologic presentations can pose diagnostic challenges, particularly when the primary tumor is unknown.
Qiannan Jia +3 more
wiley +1 more source
, 2016 Cystic hygroma and lymphangioma, currently defined as 'lymphatic malformations', are developmental abnormalities of the lymphoid system with potential for rapid expansion. The management of these abnormalities depends on the site and extent of the lesion.
LADISA, GRAZIA +5 more
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Familial renal retroperitoneal lymphangiomatosis: personal experience and review of literature
, 2010 Lymphangiomatosis of the kidneys and perirenal-retroperitoneal tissues is a rare disease of unknown etiology. We present two cases affecting members of the same family, supporting the familial nature of the disease.
G Charalampopoulos +4 more
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Orthotopic liver transplantation for massive hepatic lymphangiomatosis [PDF]
, 1988 Lymphangiomatosis is a rare malformation of the lymphatic system that causes severe symptoms secondary to progressive growth into or close to vital structures. A case report of liver failure related to this space-occupying intrahepatic mechanism is taken
Tzakis, A +17 more
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An Examination of Sirolimus's Role in Endothelial Cells of Kaposiform Haemangioendothelioma
Journal of Cellular and Molecular Medicine, Volume 29, Issue 20, October 2025.ABSTRACT Kaposiform haemangioendothelioma (KHE) research faces challenges due to the lack of established cell lines and suitable animal models. Our study aimed to establish KHE cell lines, spheroids and refine murine models to mimic disease characteristics, advancing our understanding of KHE pathogenesis and exploring novel therapies. Primary KHE cells
Yanan Li +4 more
wiley +1 more source
Management of Life-threatening Refractory Chylothorax and Chylopericardium due to Lymphangiomatosis
, 2018 Lymphangiomatosis is a rare disorder. Chylous effusion and osteolytic lesions are diagnostic clues. Radiographic findings can be suggestive of the disease, but the final confirmatory diagnosis is made histologically.
Hussam K. Hamadah, Mohamed S. Kabbani
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Journal of Hospital Medicine, Volume 21, Issue 2, Page 200-204, February 2026.
Gurpreet Dhaliwal +4 more
wiley +1 more source
Targeted Medical Therapies for Vascular Anomalies: A Clinical Review
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 199, Issue 3, Page 161-175, September 2025.ABSTRACT Vascular anomalies represent a broad spectrum of disorders characterized by aberrant blood or lymphatic vessel development, which can lead to complex clinical phenotypes. Historically, vascular anomalies were classified solely on the basis of their clinical and histopathologic features.
Whitney Eng
wiley +1 more source
Bilateral peri-renal lymphangiomatosis
Indian Journal of Urology, 2006 A 30 yrs old female with non-specific abdominal pain is presented. Ultrasound, computerised tomography abdomen were performed. A finely septated fluid collection surrounding both kidneys were found.
T P Rajeev +3 more
doaj +1 more source