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一种溶血性贫血可能掩盖另一种:阵发性夜间血红蛋白尿伪装成感染。

One Haemolytic Anaemia May Hide Another: Paroxysmal Nocturnal Haemoglobinuria Masquerading As Infection.

作者信息

Wery Alexandre-Raphael, Mortier Coline, Cabrera Quentin, Niang Mohamadou, Kone Moumini, Permal Sarah

机构信息

Department of Internal Medicine, Centre Hospitalier de Mayotte, Mamoudzou, Mayotte, France.

Department of Haematology, Centre Hospitalier Universitaire de La Réunion, Saint-Pierre, La Réunion, France.

出版信息

Eur J Case Rep Intern Med. 2024 Aug 23;11(9):004749. doi: 10.12890/2024_004749. eCollection 2024.

Abstract

BACKGROUND

Paroxysmal nocturnal haemoglobinuria (PNH) is a rare, genetic and acquired haematologic disease that causes complement-mediated intravascular haemolytic anaemia, thrombosis and bone marrow failure.

CASE DESCRIPTION

A 27-year-old migrant patient attended the emergency department in a context of fever and chills over the previous few days as well as chronic fatigue, dyspnoea and chest pain. His medical history included chronic anaemia and erectile dysfunction. Initial biology showed a haemoglobin of 6.3 g/dl, platelets of 25,000/μl, total leucocytes of 3,500/μl with 1,500 neutrophils. B12 vitamin, folic acid, ferritin and thyroid stimulating hormone were normal. Lactate dehydrogenase levels were high and haptoglobin was non-measurable. C-reactive protein was 46.1 mg/l. A thick blood smear revealed infection with 0.1% parasitaemia. The patient was treated with an oral combination of artemether and lumefantrine. Three weeks later, the patient consulted the infectious disease department given the lack of clinical improvement. The cytopenias worsened, and lactate dehydrogenase (LDH) and reticulocytes increased. Tests for schistocytes, a thick blood smear for malaria and a direct Coombs test were negative; a myelogram was reassuring. An abdominal, pelvic and thoracic CT scan showed a mild hepatomegaly with no focal lesion and no splenomegaly or adenomegaly. A 12-colour flow cytometry unveiled a PNH clone on 90.9545% of neutrophils and 80.7371% of monocytes.

DISCUSSION

PNH patients can be vulnerable to parasites infection (such as ) as it may trigger breakthrough haemolysis through uncontrolled resurgence of activity of the complement system. In our patient, infection was a confounding factor, as it commonly causes haemolytic anaemia and thrombocytopenia, and patients living in malaria-endemic regions can carry low parasitaemia while being slightly symptomatic or asymptomatic.

LEARNING POINTS

infection can cause breakthrough haemolysis in patients with paroxysmal nocturnal haemoglobinuria.Low parasitemia in patients living in malaria-endemic regions is not always significant as these patients often carry acquired immunity.Patients from malaria-endemic regions presenting with severe sickness and low parasitemia must be assessed for other diseases, as it cannot explain heavy illness.Patients presenting with haemolytic anaemia, no schistocytes, a negative direct Coombs test and other unexplained cytopenia such as thrombocytopenia/neutropenia and other unexplained clinical manifestations such as dyspnoea, chest pain or erectile dysfunction should be assessed for paroxysmal nocturnal haemoglobinuria.

摘要

背景

阵发性睡眠性血红蛋白尿(PNH)是一种罕见的、遗传性和后天获得性血液系统疾病,可导致补体介导的血管内溶血、血栓形成和骨髓衰竭。

病例描述

一名27岁的外来务工患者因前几日发热、寒战以及慢性疲劳、呼吸困难和胸痛前往急诊科就诊。他的病史包括慢性贫血和勃起功能障碍。初始血液检查显示血红蛋白为6.3 g/dl,血小板为25,000/μl,总白细胞为3,500/μl,其中中性粒细胞为1,500。维生素B12、叶酸、铁蛋白和促甲状腺激素均正常。乳酸脱氢酶水平升高,触珠蛋白无法检测到。C反应蛋白为46.1 mg/l。厚血涂片显示疟原虫感染率为0.1%。患者接受了蒿甲醚和本芴醇的口服联合治疗。三周后,由于临床症状未改善,患者前往感染科就诊。血细胞减少症加重,乳酸脱氢酶(LDH)和网织红细胞增加。裂体细胞检测、疟疾厚血涂片检查和直接抗人球蛋白试验均为阴性;骨髓检查结果令人放心。腹部、盆腔和胸部CT扫描显示轻度肝肿大,无局灶性病变,无脾肿大或淋巴结肿大。十二色流式细胞术显示90.9545%的中性粒细胞和80.7371%的单核细胞存在PNH克隆。

讨论

PNH患者可能易受寄生虫感染(如 ),因为它可能通过补体系统活性的不受控制的复苏引发突破性溶血。在我们的患者中, 感染是一个混杂因素,因为它通常会导致溶血性贫血和血小板减少,生活在疟疾流行地区的患者可能携带低疟原虫血症,同时症状轻微或无症状。

经验教训

感染可导致阵发性睡眠性血红蛋白尿患者发生突破性溶血。生活在疟疾流行地区的患者低疟原虫血症并不总是具有重要意义,因为这些患者通常具有获得性免疫力。来自疟疾流行地区且患有严重疾病和低疟原虫血症的患者必须评估是否患有其他疾病,因为低疟原虫血症无法解释严重疾病。出现溶血性贫血、无裂体细胞、直接抗人球蛋白试验阴性以及其他无法解释的血细胞减少症(如血小板减少/中性粒细胞减少)和其他无法解释的临床表现(如呼吸困难、胸痛或勃起功能障碍)的患者应评估是否患有阵发性睡眠性血红蛋白尿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b94/11379114/5d4061151d8c/4749_Fig1.jpg

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