Angiomyomatous hamartoma of lymph nodes: Clinicopathological study of 6 cases with review of literature.
Indian J Pathol Microbiol
;
2016 Apr-June 59(2): 206-208
Article
Dans Anglais
| IMSEAR
| ID: sea-179478
ABSTRACT
Angiomyomatous hamartoma (AMH) is a rare disease with predisposition for inguinal and femoral lymph nodes. Histologically, it is characterized by replacement of lymph nodal parenchyma with irregularly distributed thick walled blood vessels, haphazardly arranged smooth muscle cells, variable amount of fat and fibrous tissue in a sclerotic lymphatic stroma. Few cases have also been reported in popliteal and sub ‑ mandibular location. The exact pathogenesis is still not known. Although this entity is very rare, its recognition is important in discriminating it from other benign and malignant vascular lesions of lymph nodes.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
langue:
Anglais
Texte intégral:
Indian J Pathol Microbiol
Année:
2016
Type:
Article
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