The presence of sarcoid-type granulomata in peripheral lymph nodes, with no evidence of other typical lesions, doesn’t allow to diagnose sarcoidosis. In fact, sarcoidosis is a systemic disease and two or more organs must be affected to reach a definitive diagnosis. However this involvement could happen even several years later, thus making a correct diagnosis really difficult. In the absence of other organ involvement, an “idiopathic granulomatous disease” of peripheral lymph nodes is identified. Patients must anyway undergo a careful, long-term follow-up in order to detect clinical or radiologic variations that may confirm a diagnosis of sarcoidosis. After presenting a case-report of monolateral adenopathy of the axilla as an idiopathic granulomatous disease, the Authors review the international literature about sarcoidosis and its extra-pulmonar presentation, underlyning the importance of considering sarcoidosis among possible diagnosis when peripheral adenopathies occurr.
Linfoadenopatie ascellari monolaterali da granulomi di tipo sarcoidosico: malattia granulomatosa idiopatica o sarcoidosica? Caso clinico / Izzo, Luciano; DI CELLO, P.; Meloni, Paolo; Caputo, M.; Izzo, P.; Costi, Umberto; DE TOMA, Giorgio; Basso, Luigi; Bolognese, Antonio; Pietrasanta, Dario. - In: IL GIORNALE DI CHIRURGIA. - ISSN 0391-9005. - 5:(2008), pp. 11-22.
Linfoadenopatie ascellari monolaterali da granulomi di tipo sarcoidosico: malattia granulomatosa idiopatica o sarcoidosica? Caso clinico.
IZZO, Luciano
;MELONI, PAOLO;P. IZZO;COSTI, Umberto;DE TOMA, Giorgio;BASSO, Luigi;BOLOGNESE, Antonio;PIETRASANTA, DARIO
2008
Abstract
The presence of sarcoid-type granulomata in peripheral lymph nodes, with no evidence of other typical lesions, doesn’t allow to diagnose sarcoidosis. In fact, sarcoidosis is a systemic disease and two or more organs must be affected to reach a definitive diagnosis. However this involvement could happen even several years later, thus making a correct diagnosis really difficult. In the absence of other organ involvement, an “idiopathic granulomatous disease” of peripheral lymph nodes is identified. Patients must anyway undergo a careful, long-term follow-up in order to detect clinical or radiologic variations that may confirm a diagnosis of sarcoidosis. After presenting a case-report of monolateral adenopathy of the axilla as an idiopathic granulomatous disease, the Authors review the international literature about sarcoidosis and its extra-pulmonar presentation, underlyning the importance of considering sarcoidosis among possible diagnosis when peripheral adenopathies occurr.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.