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Generalized palisaded neutrophilic and granulomatous dermatitis—a cutaneous manifestation of chronic myelomonocytic leukemia? A clinical, histopathological, and molecular study of 3 cases

机译:广泛的促助性中性粒细胞和肉芽肿性皮炎 - 一种慢性骨髓细胞白血病的皮肤表现形式吗? 3例临床,组织病理学和分子研究

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摘要

Summary Palisaded neutrophilic and granulomatous dermatitis (PNGD) is characterized by erythematous papules or plaques on trunk or limbs and is frequently associated with rheumatologic, autoimmune, or hematologic malignancies. Histopathology shows interstitial granulomas composed of epitheloid histiocytes in the reticular dermis with surrounding foci of collagen degeneration and variable neutrophilic inflammation. We report 3 cases of generalized PNGD associated with chronic myelomonocytic leukemia (CMML), a myelodysplastic/myeloproliferative neoplasm, which may show a variety of cutaneous manifestations. SRSF2 P95 hotspot mutations, found in 40%-50% of CMML cases, were retrospectively detected in skin and bone marrow biopsies of all 3 patients, in 1 of them already 5 years before CMML diagnosis. Generalized PNGD may represent a type of cutaneous manifestation of CMML. Because diagnosis of CMML is frequently difficult in cases with isolated persistent monocytosis and minimal dysplasia in the bone marrow, patients with a generalized PNGD should be evaluated for the presence of hematologic disorders including CMML, ideally supported by mutational analyses. Highlights ? PNGD may represent a type of cutaneous manifestation of CMML. ? Patients with the pattern of PNGD should be evaluated for an underlying hematologic disorder. ? Diagnostic procedure should be supported by mutational analyses.
机译:发明内容麦克风中性粒细胞和肉芽肿性皮炎(PNGD)的特征在于躯干或四肢红斑或斑块,通常与风湿病,自身免疫或血液学恶性肿瘤相关。组织病理学表现出间隙肉芽肿组成,其与网状真皮中的上皮细胞织细胞组成,具有胶原蛋白变性和可变性嗜中性炎症的周围焦点。我们报告3例与慢性骨髓细胞白血病(CMML),一种骨髓增生/髓原瘤相关的一般性PNGD,可显示出各种皮肤表现形式。 SRSF2 P95热点突变,发现40%-50%的CMML病例,在所有3名患者的皮肤和骨髓活检中回顾性地检测到,在其中1例之前在CMML诊断前5年。广义PNGD可以代表CMML的一种皮肤表现形式。由于CMML的诊断通常难以在骨髓中分离的持续单胞增分和最小发育困难的情况下,应评估具有全血液学疾病的患者,包括CMML,理想的是通过突变分析支持。强调 ? PNGD可以代表CMML的一种无皮肤表现形式。还应评估具有PNGD模式的患者,用于潜在的血液病变。还突变分析应支持诊断程序。

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