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Posttransplant Lymphoproliferative Disease Presenting as Adrenal Insufficiency: Case Report

机译:表现为肾上腺皮质功能不全的移植后淋巴细胞增生性疾病:病例报告

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This is the first reported case of lymphoproliferative disease presenting with adrenal insufficiency after liver transplantation. A 38-year-old white man was admitted 8 months after transplantation for cryptogenic cirrhosis with fever (38-39°C), chills, cough, and dyspnea. His blood pressure was 100/70 mm Hg, there was pallor of the conjunctiva, and a lymph node was palpable in the left groin. Laboratory analyses revealed the following values: serum sodium concentration (112 mmol/L), potassium (5.4 mmol/L), hemoglobin (7.8 g/L), white blood cell count (7.7 x 109/L), glucose 3.9 (mmol/L), and mildly elevated liver functions. Abdominal ultrasound showed multiple hypoechoic solid-appearing lesions throughout the liver and spleen. Results of a biopsy specimen of the groin node confirmed polymorphic B-cell lymphoma. A negative Epstein-Barr virus screen before transplant became positive. The patient’s fever increased to 40°C. He subsequently developed sepsis and later, multiple organ failure. Autopsy confirmed extensive abdominal disease. The adrenal glands had been completely replaced by the tumor. Primary Epstein-Barr virus infection is associated with posttransplant lymphoproliferative disease. Replacement of the adrenal glands with a tumor produces a clinical picture of adrenal insufficiency.
机译:这是肝移植后首次出现淋巴增生性疾病并出现肾上腺功能不全的病例。移植后8个月,一名38岁的白人因发烧(38-39°C),发冷,咳嗽和呼吸困难的隐源性肝硬化而入院。他的血压为100/70 mm Hg,结膜苍白,左侧腹股沟可触及淋巴结。实验室分析显示以下数值:血清钠浓度(112 mmol / L),钾(5.4 mmol / L),血红蛋白(7.8 g / L),白细胞计数(7.7 x 109 / L),葡萄糖3.9(mmol / L) L),肝功能轻度升高。腹部超声检查显示,整个肝脏和脾脏均出现多发低回声的固体样病变。腹股沟淋巴结活检标本的结果证实多态性B细胞淋巴瘤。移植前阳性的爱泼斯坦-巴尔病毒筛查阴性。患者的发烧升高至40°C。随后,他患了败血症,后来发展为多器官功能衰竭。尸检证实广泛的腹部疾病。肾上腺已被肿瘤完全取代。原发性爱泼斯坦-巴尔病毒感染与移植后淋巴细胞增生性疾病有关。用肿瘤替代肾上腺产生了肾上腺功能不全的临床表现。

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