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原始细胞危象后非典型(费城染色体阴性)慢性髓性白血病的自发性脾破裂

Spontaneous splenic rupture in atypical (Philadelphia chromosome negative) chronic myeloid leukaemia following blastic crisis.

作者信息

Sachithanandan A, Gleadhill I, Alexander H D, Morris T C M

机构信息

Department of Cardiac Surgery, Royal Victoria Hospital, Belfast BT12 6BA.

出版信息

Ir Med J. 2003 Jun;96(6):181-2.

PMID:12926761
Abstract

Philadelphia chromosome negative and bcr/abl negative chronic myeloid leukaemia (CML) is an uncommon atypical CML. We describe a patient with this disorder who experienced an acute blastic transformation that resulted in rapid splenic enlargement and subsequent atraumatic splenic rupture. Clinically, spontaneous splenic rupture may be a difficult diagnosis to make and this case highlights the importance of considering atraumatic splenic rupture as a cause for unexplained abdominal pain in a patient with a haematological malignancy.

摘要

费城染色体阴性且bcr/abl阴性的慢性髓性白血病(CML)是一种罕见的非典型慢性髓性白血病。我们描述了一名患有这种疾病的患者,该患者经历了急性原始细胞转化,导致脾脏迅速肿大,随后发生非创伤性脾破裂。临床上,自发性脾破裂可能难以诊断,该病例突出了在血液系统恶性肿瘤患者中,将非创伤性脾破裂视为不明原因腹痛病因的重要性。

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Ir Med J. 2003 Jun;96(6):181-2.
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