Life threatening macrophage activation syndrome as the initial presentation of systemic lupus erythematosus: A case report and review of the literature

被引:1
|
作者
Tharwat, Samar [1 ,3 ]
Hamdy, Fatma [1 ]
Abdelzaher, Mohamed Gamal [1 ]
Bakr, Leila [1 ]
El Hassany, Aya [1 ]
Abdelsattar, Mostafa [1 ]
Eldesoky, Rehab T. [2 ]
Ibrahim, Eman M. [2 ]
机构
[1] Mansoura Univ, Fac Med, Dept Internal Med, Rheumatol & Immunol Unit, Mansoura, Egypt
[2] Mansoura Univ, Fac Med, Dept Pathol, Mansoura, Egypt
[3] Mansoura Univ Hosp, Rheumatol & Immunol, Rheumatol & Immunol Unit, Internal Med Dept, Mansoura, Dakahlia, Egypt
来源
EGYPTIAN RHEUMATOLOGIST | 2023年 / 45卷 / 01期
关键词
Systemic lupus erythematosus; Macrophage activation syndrome; Fever; JUVENILE IDIOPATHIC ARTHRITIS; HEMOPHAGOCYTIC SYNDROME; CLASSIFICATION CRITERIA; MULTICENTER; CHILDREN; ONSET; PATHOPHYSIOLOGY; MANIFESTATION; DIAGNOSIS; DISEASES;
D O I
10.1016/j.ejr.2022.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Macrophage activation syndrome (MAS) is characterized by activation of hemophagocytic cells and is a very rare initial manifestation of systemic lupus erythematosus (SLE). Aim of the work: To describe the features of a challenging case of SLE initially presented with MAS.Case report: A previously healthy 20-year-old female was referred to the Rheumatology clinic with a 25 -days' history of persistent fever, general fatigue, and significant weight loss. Clinical examination revealed a high-grade fever (41 degrees C), significant hair loss and general malaise. Laboratory investigations revealed leucopenia (1.5 x 109/L), neutropenia (0.7 x 109/L), lymphopenia (0.6 x 109/L), normocytic nor-mochromic anemia (9 g/dL), thrombocytopenia (95 x 109/L), elevated liver enzymes, hyperbilirubinemia (2.6 mg/dl); hypertriglyceridemia (306 mg/dL), hyperferritinemia (16000 ng/mL), elevated D-Dimer (4.7 mg/L), elevated lactate dehydrogenase (1379 U/L) and direct and indirect Coombs' tests were posi-tive. Erythrocyte sedimentation rate was 28 mm/1st h. Immunological screening was positive for antin-uclear antibody (ANA) and anti-double stranded deoxyribonucleic acid (anti-dsDNA). Serum C3 and C4 complement factors were low and C reactive protein was negative. Soluble CD25 was elevated (9800 pg/ml). Bone marrow biopsy showed hypocellular bone marrow with normal megakaryocytes and erythroid series with evidence of hemophagocytosis. A diagnosis of SLE initially presented with MAS was made. The patient received intravenous methylprednisolone for 5 consecutive days followed by prednisolone and cyclosporine A and intravenous immunoglobulin. The condition deteriorated with progressive coagulopathy, thrombocytopenia and hyperferritinemia. Subsequently, the conscious level of the patient deteriorated, multiorgan failure developed and the patient died.Conclusion: MAS is a serious condition that may be the first presentation of SLE.(c) 2022 THE AUTHORS. Publishing services by ELSEVIER B.V. on behalf of The Egyptian Society of Rheu-matic Diseases. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:45 / 49
页数:5
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