Sarcoidosis presenting with bicytopenia due to bone marrow granuloma

IF 0.1 Q4 HEMATOLOGY Iraqi Journal of Hematology Pub Date : 2023-10-16 DOI:10.4103/ijh.ijh_62_23
Mansoor C. Abdulla
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Abstract

Abstract: A 55-year-old homemaker presented with low-grade fever, fatigue, and loss of weight for 2 months. She had hepatosplenomegaly, mediastinal lymphadenopathy, cytopenias, hypercalcemia with normal parathormone, and noncaseating granulomas in bone marrow and lymph node biopsy. The patient was diagnosed to have sarcoidosis with bone marrow involvement (histopathology showing noncaseating granuloma and high serum angiotensin-converting enzyme after ruling out other causes of granulomatous disorders by appropriate tests). She was managed with prednisolone 20 mg daily which was reduced and stopped after 3 months. On follow-up, she was asymptomatic and her blood counts were normal. Diagnosis of sarcoidosis should be considered always after ruling out other causes since it can mimic lymphoproliferative disorders and granulomatous infections. The initial presentation of sarcoidosis with bicytopenia due to bone marrow granulomas is extremely rare and physicians should have awareness of such atypical presentations.
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骨髓肉芽肿引起的结节病表现为双氧体减少症
摘要:55岁家庭主妇,以低烧、乏力、体重下降2个月为临床表现。她有肝脾肿大,纵隔淋巴结病,细胞减少,高钙血症伴甲状旁腺激素正常,骨髓和淋巴结活检显示非干酪化肉芽肿。患者被诊断为结节病伴骨髓浸润(组织病理学显示非干酪化肉芽肿和高血清血管紧张素转换酶,经适当检查排除肉芽肿疾病的其他原因)。患者每日使用强的松龙20mg, 3个月后减量停用。在随访中,她无症状,血液计数正常。结节病的诊断应在排除其他原因后考虑,因为它可以模拟淋巴增生性疾病和肉芽肿感染。骨髓肉芽肿引起的双氧体减少的结节病的最初表现是非常罕见的,医生应该意识到这种不典型的表现。
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