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Lymphomatoid granulomatosis presenting with cutaneous involvement: a case report and review of the literature

机译:淋巴瘤样肉芽肿伴皮肤受累:一例报道并文献复习

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摘要

Lymphomatoid granulomatosis (LG) is a rare Epstein-Barr virus (EBV)-associated B-cell lymphoproliferative disorder presenting in middle adulthood that nearly always affects the lungs and shows cutaneous involvement in up to 50% of cases. Skin lesions are present at the time of diagnosis in roughly one-third of patients and may precede the development of lung lesions in as many as 10-15%. Recognition by both the dermatologist and dermatopathologist is therefore crucial for early and accurate diagnosis. While skin involvement is grossly and microscopically diverse, the disease most commonly presents as erythematous subcutaneous and dermal nodules showing the classic histopathologic triad of transmural lymphocytic angiitis, atypical B-lymphocytes in a polymorphous T-cell background, and necrotic foci within lymphoid aggregates. We present a case of lymphomatoid granulomatosis initially presenting with cutaneous lesions, with an accompanying review of the literature.
机译:淋巴结肉芽肿病(LG)是一种罕见的与爱泼斯坦-巴尔病毒(EBV)相关的B细胞淋巴组织增生性疾病,在成年中期出现,几乎总是影响肺部,在多达50%的病例中显示皮肤受累。在诊断时大约三分之一的患者存在皮肤病变,可能在肺部病变发生之前占10-15%。因此,皮肤科医生和皮肤病理学家的识别对于早期和准确的诊断至关重要。尽管皮肤受累的情况在微观上千差万别,但该病最常见的表现为皮下和皮肤红斑结节,表现出典型的组织病理学三联征,即透壁性淋巴细胞性血管炎,多形T细胞背景中的非典型B淋巴细胞以及淋巴样聚集物中的坏死灶。我们提出一例淋巴瘤样肉芽肿病,最初表现为皮肤病变,并伴有文献综述。

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