Acute Panmyelosis with Myelofibrosis: An Unusual Cause of Pancytopenia

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
E. Tseng, F. Moid, J. Blondal, Jerry M Maniate
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引用次数: 0

Abstract

A 56-year-old woman presented to her family physician with a 2-month history of dizziness, palpitations, dyspnea on exertion,and episodic chest discomfort. Initial investigations revealed amild pancytopenia. Two days later, she presented to emergencywith a low-grade fever (37.8oC), left-sided chest discomfort, andweakness. She denied any infectious or bleeding symptoms andhad no significant past medical history, including no medications. On examination, the patient had no lymphadenopathy, andher cardiac, respiratory, and abdominal examinations were unre-markable, with no hepatosplenomegaly. Her investigationsrevealed a pancytopenia (see Table 1). On the basis of her neu -tropenia and low-grade fever, she was admitted for intravenousantibiotics and work-up of her pancytopenia.In hospital, her pancytopenia persisted; her counts reached anadir of hemoglobin (Hgb) 46 g/L, platelets (Plt) 16 X 10
急性骨髓增生伴骨髓纤维化:全血细胞减少症的一种不寻常原因
一名56岁女性向家庭医生就诊,有2个月的头晕、心悸、用力时呼吸困难和间歇性胸部不适病史。初步调查显示轻度全血细胞减少症。两天后,患者出现低烧(37.8℃)、左侧胸部不适和虚弱。她否认有任何感染或出血症状,没有明显的既往病史,包括没有服用药物。检查时,患者无淋巴结病变,心脏、呼吸和腹部检查无明显异常,无肝脾肿大。她的检查显示有全血细胞减少症(见表1)。根据她的新肌减少症和低烧,她被静脉注射抗生素并检查了她的全血细胞减少症。在医院里,她的全血细胞减少症持续存在;血红蛋白(Hgb) 46 g/L,血小板(Plt) 16 X 10
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来源期刊
University of Toronto Medical Journal
University of Toronto Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
0.30
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0.00%
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