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The Pathologic Findings of Skin Lymph Node Liver and Bone Marrow in Patients With Adult-Onset Still Disease

机译:成年静止性疾病患者皮肤淋巴结肝和骨髓的病理发现

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摘要

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.
机译:成人发作性静止疾病(AOSD)的特征是发烧,皮疹和淋巴结病,伴有白细胞增多和贫血,这是实验室常见的发现。我们调查了皮肤,淋巴结,肝脏和骨髓的特征性病理发现,以辅助AOSD的正确诊断。该研究纳入了40名AOSD患者。回顾性分析1998年至2013年间的皮肤(26例),淋巴结(8例),肝脏(8例)或骨髓活检(22例)。在排除常见感染,血液和自身免疫性疾病后,根据Yamaguchi标准诊断了AOSD患者。进行了免疫组织化学,免疫荧光和爱泼斯坦-巴尔病毒编码的RNA(EBER)原位杂交。大多数皮肤活检显示上层真皮有轻度淋巴细胞或组织细胞浸润。真皮中经常发现核碎片14例(53.8%)。一半以上的病例(n = 14,53.8%)显示出间质粘蛋白沉积。有些病例表现为界面性皮炎伴角质形成细胞坏死或基底空泡形成(n = 10,38.5%)。淋巴结活检显示皮层旁或弥漫性增生,伴有免疫母细胞和血管增生。肝活检显示稀疏的门脉和窦性炎症细胞浸润。所有病例均显示不同程度的库普弗细胞增生。骨髓的细胞密度从20%到80%不等。 22例病例中有14例发现髓样细胞增生(63.6%)。免疫组织化学分析显示,皮肤,肝脏和骨髓中CD8阳性淋巴细胞的数目大于CD4阳性淋巴细胞的数目,但淋巴结中CD4阳性淋巴细胞的数目大于CD8阳性淋巴细胞的数目关于AOSD的皮肤表现的相对具体发现是上层真皮中的轻度炎性细胞浸润,基底空泡化,角质形成细胞坏死,真皮中存在核淋巴结炎和粘蛋白。在所有情况下,淋巴结的病理结果包括皮质旁增生以及血管和免疫母细胞增生。除临床发现外,皮肤和淋巴结病理还可以帮助诊断AOSD。

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