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以免疫性血小板减少性紫癜为表现的结核病

Tuberculosis presenting as immune thrombocytopenic purpura.

作者信息

al-Majed S A, al-Momen A K, al-Kassimi F A, al-Zeer A, Kambal A M, Baaqil H

机构信息

College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Acta Haematol. 1995;94(3):135-8. doi: 10.1159/000203995.

Abstract

Various haematological abnormalities commonly occur in active tuberculosis (TB). However, thrombocytopenia is rare and immune thrombocytopenic purpura (ITP) is mentioned only in few case reports. We found that of 846 cases with active TB, 9 (1%) presented with ITP as the only abnormality. Three out of these 9 cases had disseminated miliary TB, 3 an abdominal abscess or lymphadenitis, and 3 pulmonary TB; none had palpable splenomegaly. All patients had purpura and the platelet count varied between 4 and 21 x 10(9)/l, and the bone marrow showed increased megakaryocytes. All tuberculous patients showed initially a poor platelet count response to steroid therapy. The platelet count returned to normal 2-6 weeks after oral prednisone combined with antituberculous drugs.

摘要

各种血液学异常在活动性结核病(TB)中很常见。然而,血小板减少症很少见,免疫性血小板减少性紫癜(ITP)仅在少数病例报告中被提及。我们发现,在846例活动性结核病例中,9例(1%)仅表现为ITP这一异常。这9例中有3例为播散性粟粒型结核,3例为腹部脓肿或淋巴结炎,3例为肺结核;均无脾脏肿大可触及。所有患者均有紫癜,血小板计数在4至21×10⁹/L之间,骨髓显示巨核细胞增多。所有结核患者最初对类固醇治疗的血小板计数反应较差。口服泼尼松联合抗结核药物后2至6周血小板计数恢复正常。

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