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[非霍奇金淋巴瘤酷似米库利奇病:一例报告]

[Non-Hodgkin's lymphoma mimicking Mikulicz disease: a case report].

作者信息

Liu A C, Chen Y, Jia J S, Gao S Y, Liu Y Y

机构信息

Department of Kidney, Peking University People's Hospital, Beijing 100044, China.

Rehabilitation Centre for Chronic Disease, Taihe Hospital, Shiyan 442000, Hubei, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2016 Dec 18;48(6):1074-1076.

Abstract

IgG4-related disease is a systemic disorder involving a spectrum of multiple indications, and various histopathological features are shared among different IgG4-related disease subtypes, which challenge diagnosis, although certain syndromes have organ-specific involvement. Among them, Mikulicz's disease affecting the salivary and lacrimal glands, distinguished by often elevated levels of serum IgG4, infiltration of IgG4 plasma cells into target tissues, and diffuse swelling, mass formation, or fibrosis of affected organs. However, there are several diseases, which could manifest as salivary gland swelling, mimicking Mikulicz's disease, such as Sjogren's syndrome, mumps virus infection, obstruction of parotid duct, non-Hodgkin's lymphoma (NHL), and so on. So differential diagnosis is important and essential as to the salivary gland swelling. In this paper, we analyzed a case of a 59-year-old male with symmetric salivary gland swelling. Mikulicz's disease was misdiagnosed at the beginning without biopsy. Prednisone treatment ever seemed to be effective and antibiotics had no effect. Besides salivary involvement, the patient also manifested as testicle swelling and severe pancytopenia with the development of the disease, which rarely appeared in Mikulicz's disease. Physical examination showed skin, sclera yellow dye, swollen submandibular, sublingual and lacrimal gland and splenomegaly. As a result, biopsy of right submandibular gland was made, and mucosa-associated lymphoid tissue lymphoma was confirmed by morphology and immunohistochemistry. Bone marrow biopsy also confirmed that lymphoma cells were found in the bone marrow. Finally, the diagnosis of mucosa-associated lymphoid tissue lymphoma (Phase IVE, Group A) was made on the patient, who was transferred to the hematology department for the treatment. NHL, especially, primary extranodal lymphoma usually involves the salivary gland, and painless swelling of the salivary gland is a common manifestation, similar with Mikulicz's disease. So although salivary gland swelling is often associated with autoimmune diseases such as Sjogren's syndrome and IgG4-related disease, the awareness and suspicion of a possibility of NHL are essential for rheumatologists. Biopsy is a necessary examination to decrease or avoid misdiagnosis.

摘要

IgG4相关性疾病是一种涉及多种临床表现谱的全身性疾病,不同IgG4相关性疾病亚型具有多种共同的组织病理学特征,这对诊断构成挑战,尽管某些综合征有器官特异性受累情况。其中,米库利奇病累及唾液腺和泪腺,其特征通常为血清IgG4水平升高、IgG4浆细胞浸润靶组织以及受累器官弥漫性肿胀、肿块形成或纤维化。然而,有几种疾病可表现为唾液腺肿胀,酷似米库利奇病,如干燥综合征、腮腺炎病毒感染、腮腺导管阻塞、非霍奇金淋巴瘤(NHL)等。因此,对于唾液腺肿胀进行鉴别诊断非常重要且必要。在本文中,我们分析了一例59岁男性对称性唾液腺肿胀的病例。该患者最初未进行活检而被误诊为米库利奇病。泼尼松治疗曾似乎有效,而抗生素治疗无效。随着病情发展,除唾液腺受累外,患者还表现为睾丸肿胀和严重全血细胞减少,这在米库利奇病中很少出现。体格检查显示皮肤、巩膜黄染,下颌下腺、舌下腺和泪腺肿大以及脾肿大。因此,对右侧下颌下腺进行了活检,通过形态学和免疫组织化学确诊为黏膜相关淋巴组织淋巴瘤。骨髓活检也证实骨髓中发现淋巴瘤细胞。最终,该患者被诊断为黏膜相关淋巴组织淋巴瘤(IV期E组,A类),并转至血液科进行治疗。特别是NHL,原发性结外淋巴瘤通常累及唾液腺,唾液腺无痛性肿胀是常见表现,与米库利奇病相似。所以,尽管唾液腺肿胀常与自身免疫性疾病如干燥综合征和IgG4相关性疾病相关,但风湿科医生必须意识到并怀疑NHL的可能性。活检是减少或避免误诊的必要检查。

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