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抗黑色素瘤分化相关基因5抗体阳性皮肌炎中的致死性广泛性多器官出血:一例尸检病例报告

Fatal and extensive multiorgan hemorrhages in anti-melanoma differentiation-associated gene 5 antibody-positive dermatomyositis: An autopsy case report.

作者信息

Watanabe Tsuyoshi, Takizawa Naoho, Nagasaka Toru, Nakamura Yoshihiro, Ikai Hiroki, Yamamoto Mari, Murai Yukari, Takasugi Koji, Yokoyama-Kokuryo Waka, Fujita Yoshiro

机构信息

Department of Rheumatology.

Department of Pathology.

出版信息

Medicine (Baltimore). 2020 Jan;99(3):e18600. doi: 10.1097/MD.0000000000018600.

Abstract

INTRODUCTION

Anti-melanoma differentiation-associated gene 5 antibody (anti-MDA5 Ab) is an autoantigen associated with dermatomyositis (DM). Anti-MDA5 Ab-positive DM patients frequently exhibit clinically amyopathic dermatomyositis (CADM), and develop rapidly progressive interstitial lung disease (RPILD). Even with early detection and potent combination immunosuppressive therapy, anti-MDA5 Ab-positive DM patients have a poor prognosis. In the present case report, we present a rare autopsy case of a patient with anti-MDA5 Ab DM with RPILD who exhibited diffuse alveolar damage (DAD) patterning in lung specimens, and extensive hemorrhages in multiple organs.

PATIENT CONCERNS

An 82-year-old Japanese man admitted with bacterial pneumonia was subsequently diagnosed with anti-MDA5 Ab-positive DM based on skin manifestations (mechanic's hand, ulcerated palmar papules, and flagellate erythema), myositis, interstitial pneumonia, and elevation of anti-MDA5 Ab titer.

DIAGNOSIS

The patient was diagnosed with anti-MDA5 Ab DM, complicated with RPILD.

INTERVENTIONS

The patient received potent immunosuppressive therapy consisting of pulse methylpredonisolone at a dose of 1000 mg for 3 days, followed by prednisolone at 60 mg/d, a 1000 mg pulse of intravenous cyclophosphamide (IVCY), and oral tacrolimus at 6 mg/d. Intravenous immunoglobulin (IVIG) at a dose of 400 mg/kg/d for 5 days was subsequently administered.

OUTCOMES

Despite triple immunosuppressive therapy and IVIG, the patients' respiratory status deteriorated, and the patient died of respiratory failure on the twelfth day after admission. An autopsy revealed pulmonary DAD and multiorgan hemorrhages, including the left iliopsoas muscle, gastric and bowl mucosa, spleen, and left adrenal gland.

LESSONS

Multiorgan hemorrhages may be a fatal complication in anti-MDA5 Ab DM patients.

摘要

引言

抗黑色素瘤分化相关基因5抗体(抗MDA5抗体)是一种与皮肌炎(DM)相关的自身抗原。抗MDA5抗体阳性的DM患者常表现为临床无肌病性皮肌炎(CADM),并发展为快速进展性间质性肺病(RPILD)。即使早期发现并采用强效联合免疫抑制治疗,抗MDA5抗体阳性的DM患者预后仍较差。在本病例报告中,我们展示了一例罕见的抗MDA5抗体DM合并RPILD患者的尸检病例,该患者肺部标本显示弥漫性肺泡损伤(DAD)模式,多个器官有广泛出血。

患者情况

一名82岁日本男性因细菌性肺炎入院,随后根据皮肤表现(技工手、手掌丘疹溃疡和鞭状红斑)、肌炎、间质性肺炎及抗MDA5抗体滴度升高被诊断为抗MDA5抗体阳性的DM。

诊断

患者被诊断为抗MDA5抗体DM,合并RPILD。

干预措施

患者接受了强效免疫抑制治疗,包括静脉注射1000mg甲泼尼龙冲击治疗3天,随后口服泼尼松龙60mg/d,静脉注射1000mg环磷酰胺(IVCY)冲击治疗,以及口服他克莫司6mg/d。随后给予静脉注射免疫球蛋白(IVIG),剂量为400mg/kg/d,共5天。

结果

尽管采用了三联免疫抑制治疗和IVIG,患者的呼吸状况仍恶化,入院第12天死于呼吸衰竭。尸检显示肺部DAD及多器官出血,包括左髂腰肌、胃和肠黏膜、脾脏及左肾上腺。

经验教训

多器官出血可能是抗MDA5抗体DM患者的致命并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0606/7220071/c60a84e4fab3/medi-99-e18600-g001.jpg

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