Henoch-Schönlein syndrome (HSS) is a systemic necrotizing vasculitis predominantly affecting children. Symptoms are usually self-limited and only rarely do they involve the central nervous system. Only five published reports describe cases of radiologically proven intracranial hemorrhages complicating HSS. In this 17-year-old boy, a cerebellar hemorrhage developed after aspecific symptoms of upper respiratory tract infection. His past medical history and emerging evidence of systemic bleeding yielded a diagnosis of recurrent HSS. This was the fourth time the disease had recurred since the age of 4. The patient underwent surgical treatment and returned to his normal activities.
Henoch-Schönlein syndrome and cerebellar hemorrhage: report of an adolescent case and literature review / Paolini, Sergio; Ciappetta, Pasqualino; Piattella, M. C.; Domenicucci, Maurizio. - In: SURGICAL NEUROLOGY. - ISSN 0090-3019. - STAMPA. - 60:4(2003), pp. 339-342. [10.1016/S0090-3019(03)00166-6]
Henoch-Schönlein syndrome and cerebellar hemorrhage: report of an adolescent case and literature review.
PAOLINI, SERGIO;CIAPPETTA, Pasqualino;DOMENICUCCI, Maurizio
2003
Abstract
Henoch-Schönlein syndrome (HSS) is a systemic necrotizing vasculitis predominantly affecting children. Symptoms are usually self-limited and only rarely do they involve the central nervous system. Only five published reports describe cases of radiologically proven intracranial hemorrhages complicating HSS. In this 17-year-old boy, a cerebellar hemorrhage developed after aspecific symptoms of upper respiratory tract infection. His past medical history and emerging evidence of systemic bleeding yielded a diagnosis of recurrent HSS. This was the fourth time the disease had recurred since the age of 4. The patient underwent surgical treatment and returned to his normal activities.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.