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结节性肺淀粉样变:干燥综合征的一种表现

Nodular Pulmonary Amyloidosis: A Manifestation of Sjögren's Syndrome.

作者信息

Gómez Correa Gustavo Adolfo, Osorno Serna Jovani, Cáceres Acosta Manuel Felipe, Cáceres González Juan David, Calle Ramirez Jaime Andrés, Sandoval Mesa Juan Paulo, Roldán Pérez Miguel Ignacio

机构信息

Specialist in Internal Medicine and Pneumology, Department of Internal Medicine, Universidad de Antioquia, San Vicente Foundation University Hospital, Colombia.

Specialist in Internal Medicine, Pneumology, Thoracic Oncology and Epidemiology, Department of Internal Medicine, Universidad de Antioquia, San Vicente Foundation University Hospital, Colombia.

出版信息

Case Rep Pulmonol. 2018 Aug 13;2018:9745935. doi: 10.1155/2018/9745935. eCollection 2018.

Abstract

CASE DESCRIPTION

A 72-year-old woman with primary Sjögren Syndrome (SS) was diagnosed during an inpatient hospital stay with dry symptoms. The patient had respiratory and constitutional symptoms, requiring a pulmonary imaging evaluation by high-resolution computed tomography (HRCT) of the thorax.

CLINICAL FINDINGS

Multiple cavitary pulmonary nodules, halo sign, and focal areas of ground-glass opacity with predominance in both bases were found in the images. Complementary studies were done where a neoplastic focus was ruled out. The diagnosis of nodular pulmonary amyloidosis was confirmed with a pulmonary biopsy performed by videothoracoscopy for histopathological study, which reported the formation of nodules in the parenchyma with amyloid deposits and positive immunohistochemical markers for CD3, CD20, and CD38 lymphocytic infiltration.

TREATMENT AND OUTCOME

Initial inpatient management with intravenous cyclophosphamide and methylprednisolone was given. Subsequent outpatient management was given with high dose glucocorticoids.

CLINICAL RELEVANCE

We presented a case of nodular pulmonary amyloidosis in a female patient with primary SS, which is a rare pulmonary manifestation of this syndrome.

摘要

病例描述

一名72岁患有原发性干燥综合征(SS)的女性患者在住院期间因出现干燥症状而被诊断。该患者有呼吸和全身症状,需要通过胸部高分辨率计算机断层扫描(HRCT)进行肺部影像学评估。

临床发现

图像中发现多个空洞性肺结节、晕征以及以双肺底部为主的局灶性磨玻璃影。进行了相关补充检查,排除了肿瘤病灶。通过电视胸腔镜肺活检进行组织病理学研究,确诊为结节性肺淀粉样变性,报告显示实质内有结节形成,伴有淀粉样沉积,免疫组化标记物显示CD3、CD20和CD38淋巴细胞浸润阳性。

治疗与结果

最初给予静脉注射环磷酰胺和甲基泼尼松龙进行住院治疗。随后门诊给予高剂量糖皮质激素治疗。

临床意义

我们报告了一例原发性SS女性患者的结节性肺淀粉样变性病例,这是该综合征罕见的肺部表现。

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