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International Journal of Advances In Case Reports

Volume 11, Issue 1, 2024
Mcmed International
International Journal of Advances In Case Reports
Issn
XXX-XXXX (Print), 2349 - 8005 (Online)
Frequency
bi-annual
Email
editorijacr@mcmed.us
Journal Home page
http://mcmed.us/about/ijacr
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Abstract
Title
ANGIOMYOLIPOMATOUS HAMARTOMA - A CASE REPORT WITH REVIEW OF LITERATURE
Author
Margaret Theresa, Fathima Jackia Banu I
Email
drgerie@gmail.com
keyword
Angiomyolipomatous Hamartoma, Benign Vascular Tumor, Inguinal Lymph Node
Abstract
Angiomyolipomatous hamartoma is a rare benign vascular disease. The tumor is characterised by replacement of parenchymal lymphoid tissue by blood vessels, adipose tissue, smooth muscle and fibrous tissue. The most common lymph node involved are inguinal and femoral lymph nodes. Angiomyolipomatous hamartoma has a wide range of age distribution ranging from 8 months to 89 years with male predominance. The common clinical presentations are painless, non-tender and mobile mass. Angiomyolipomatous hamartoma is important to recognise because it clinically mimic various tumors. Differential diagnosis to be considered are lymphangiomatosis, leiomyomatosis and angiomyolipoma of lymph node. We described angiomyolipomatous hamartoma keeping in mind its unusual occurance and in order to elucidate its biological potential and histogenesis
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