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成人斯蒂尔病患者皮肤、淋巴结、肝脏及骨髓的病理表现:40例病例综合分析

The pathologic findings of skin, lymph node, liver, and bone marrow in patients with adult-onset still disease: a comprehensive analysis of 40 cases.

作者信息

Kim Hyoun-Ah, Kwon Jee Eun, Yim Hyunee, Suh Chang-Hee, Jung Ju-Yang, Han Jae Ho

机构信息

From the Department of Rheumatology (H-AK, C-HS, J-YJ); and Department of Pathology (JEK, HY, JHH), Ajou University School of Medicine, Suwon, Korea.

出版信息

Medicine (Baltimore). 2015 May;94(17):e787. doi: 10.1097/MD.0000000000000787.

Abstract

Adult-onset Still disease (AOSD) is characterized by fever, skin rash, and lymphadenopathy with leukocytosis and anemia as common laboratory findings. We investigated the characteristic pathologic findings of skin, lymph node, liver, and bone marrow to assist in proper diagnosis of AOSD.Forty AOSD patients were included in the study. The skin (26 patients), lymph node (8 patients), liver (8 patients), or bone marrow biopsies (22 patients) between 1998 and 2013 were retrospectively analyzed. AOSD patients were diagnosed according to the Yamaguchi criteria after excluding common infections, hematological and autoimmune diseases. Immunohistochemistry, immunofluorescence, and Epstein-Barr virus-encoded RNA (EBER) in situ hybridization were performed.Most skin biopsies revealed mild lymphocytic or histiocytic infiltration in the upper dermis. Nuclear debris was frequently found in the dermis in 14 cases (53.8%). More than half of the cases (n = 14, 53.8%) showed interstitial mucin deposition. Some cases showed interface dermatitis with keratinocyte necrosis or basal vacuolization (n = 10; 38.5%). The lymph node biopsies showed a paracortical or diffuse hyperplasia pattern with immunoblastic and vascular proliferation. The liver biopsies showed sparse portal and sinusoidal inflammatory cell infiltration. All cases showed various degrees of Kupffer cell hyperplasia. The cellularity of bone marrow varied from 20% to 80%. Myeloid cell hyperplasia was found in 14 out of the 22 cases (63.6%). On immunohistochemistry, the number of CD8-positive lymphocytes was greater than that of CD4-positive lymphocytes in the skin, liver, and bone marrow, but the number of CD4-positive lymphocytes was greater than that of CD8-positive lymphocytes in the lymph nodes.The relatively specific findings with respect to the cutaneous manifestation of AOSD were mild inflammatory cell infiltration in the upper dermis, basal vacuolization, keratinocyte necrosis, presence of karyorrhexis, and mucin in the dermis. In all cases, pathologic findings in the lymph nodes included paracortical hyperplasia with vascular and immunoblastic proliferation. Skin and lymph node pathology in addition to clinical findings can aid in the diagnosis of AOSD.

摘要

成人斯蒂尔病(AOSD)的特征为发热、皮疹、淋巴结病,白细胞增多和贫血是常见的实验室检查结果。我们研究了皮肤、淋巴结、肝脏和骨髓的特征性病理表现,以协助AOSD的正确诊断。

本研究纳入了40例AOSD患者。对1998年至2013年间的皮肤活检(26例患者)、淋巴结活检(8例患者)、肝脏活检(8例患者)或骨髓活检(22例患者)进行了回顾性分析。在排除常见感染、血液系统疾病和自身免疫性疾病后,根据山口标准诊断AOSD患者。进行了免疫组织化学、免疫荧光和爱泼斯坦-巴尔病毒编码RNA(EBER)原位杂交检测。

大多数皮肤活检显示真皮浅层有轻度淋巴细胞或组织细胞浸润。14例(53.8%)在真皮中经常发现核碎片。超过半数病例(n = 14,53.8%)显示间质黏蛋白沉积。部分病例表现为界面性皮炎伴角质形成细胞坏死或基底空泡化(n = 10;38.5%)。淋巴结活检显示副皮质区或弥漫性增生模式,伴有免疫母细胞和血管增生。肝脏活检显示门静脉和肝血窦有稀疏的炎性细胞浸润。所有病例均显示不同程度的库普弗细胞增生。骨髓细胞含量在20%至80%之间。22例中有14例(63.6%)发现髓样细胞增生。免疫组织化学检测显示,皮肤、肝脏和骨髓中CD8阳性淋巴细胞数量多于CD4阳性淋巴细胞,但淋巴结中CD4阳性淋巴细胞数量多于CD8阳性淋巴细胞。

AOSD皮肤表现的相对特异性表现为真皮浅层轻度炎性细胞浸润、基底空泡化、角质形成细胞坏死、核碎裂以及真皮内黏蛋白。所有病例中,淋巴结的病理表现包括副皮质区增生伴血管和免疫母细胞增生。除临床症状外,皮肤和淋巴结病理检查有助于AOSD的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8725/4603035/e621d94cdbdc/medi-94-e787-g003.jpg

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