McCrindle B W, Wood R A, Nussbaum A R
Department of Pediatrics, Johns Hopkins Hospital, Baltimore, MD 21205.
Clin Pediatr (Phila). 1988 May;27(5):254-6. doi: 10.1177/000992288802700509.
Henoch-Schönlein Syndrome (HSS) is characterized by the presence of purpuric skin lesions, colicky abdominal pain, renal manifestations, and arthritis. We report a case complicated by several unusual manifestations, including hydrops of the gallbladder and extreme thrombocytosis. Gallbladder hydrops has been known to occur in association with several conditions including Kawasaki syndrome, scarlet fever, and leptospirosis, but no previous report of this occurring in a patient with HSS could be found. The hydrops in our patient resolved spontaneously without specific medical or surgical treatment.
过敏性紫癜（HSS）的特征是出现紫癜性皮肤病变、绞痛性腹痛、肾脏表现和关节炎。我们报告一例伴有几种不寻常表现的病例，包括胆囊积液和极度血小板增多症。已知胆囊积液可与多种疾病相关，包括川崎病、猩红热和钩端螺旋体病，但此前未发现有HSS患者出现这种情况的报告。我们患者的胆囊积液未经特殊药物或手术治疗即自行消退。
