Autor: |
IACONETTA, G., FRISCIA, M., DELL''AVERSANA ORABONA, G., DE BIASI, S., ROMANO, A., PIOMBINO, P., GRAZIANO, P., ABBATE, V., SALZANO, G., MAGLITTO, F., CALIFANO, L. |
Zdroj: |
European Review for Medical & Pharmacological Sciences; Apr2014, Vol. 18 Issue 8, p1241-1246, 6p |
Abstrakt: |
Castleman's disease (giant lymph node hyperplasia, angiofollicular hyperplasia, lymphoid hamartoma, benign giant lymphoma), is a quite rare and complex disease of lymphoid tissue that causes progressive lymph node enlargement, typically presenting as a solitary mediastinal mass. It was first described by Castleman et al in 1956. The head and neck regions are the second, less common site for this lesion. The preoperative diagnosis is very often extremely difficult and the routine investigations are often inconclusive. A multicentric extension of this disease shows poorer prognosis compared to the unifocal Histologically, three types do exist: the hyaline-vascular type, the plasma cell type and the mixed type. The etiology and pathogenesis is still unclear. In the literature, to our knowledge, only 112 cases have been reported involving head and neck, and only 22, including our own, interesting the parotid gland. In this report we describe a rare singular of Castleman's disease presenting as a tumor of the inferior pole of the parotid gland extending in the submandibular region, in a 35-year-old woman. The patient undergone a surgical treatment and, therefore, the mass was successfully totally removed. [ABSTRACT FROM AUTHOR] |
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