Traumatic Ulcerative Granuloma with Stromal Eosinophilia: From Reactive Process to Low Grade CD30 + lymphoproliferative Disorder.

Rachelle Wolk, Denise Trochesset
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Abstract

Purpose of review: Traumatic ulcerative granuloma with stromal eosinophilia (TUGSE) is a rare, benign ulcerative lesion of the oral mucosa that exists in both adult and infantile (Riga-Fede) forms. This review examines TUGSE by exploring its clinical presentation, pathogenesis, histopathological features, and treatment approaches. It briefly discusses oral CD30+ T-cell lymphoproliferative disorders (TLPDs) and their potential relation with TUGSE lesions.

Recent findings: While traditionally considered reactive in nature, some recent evidence suggests TUGSE may share features with CD30+ T-cell lymphoproliferative disorders (TLPDs), potentially representing a spectrum of lesions and thereby complicating diagnosis and treatment approaches. Although some TUGSE cases demonstrate CD30 positivity and monoclonality of the T-cell receptor gamma (TCRγ) chain gene, no cases have progressed to widespread or systemic lymphoma. The rarely reported CD30+ TLPDs of the oral cavity appear to share features with their cutaneous counterparts, demonstrating indolent biologic behavior and excellent prognosis, with complete or partial regression frequently occurring after incisional biopsy. TUGSE presents as a slow-healing ulcer with raised borders and induration, commonly affecting the tongue and potentially mimicking squamous cell carcinoma. While trauma appears to be an important factor, the exact pathogenesis remains unclear. Histopathologically, lesions show ulceration with polymorphous infiltrate rich in eosinophils extending into the submucosa, with characteristic muscle fiber degeneration and variable presence of atypical mononuclear cells. The condition generally follows a self-limiting course with excellent prognosis, responding well to conservative management. Aggressive treatment and extensive follow-up may be unnecessary even for CD30+ cases with monoclonal TCRγ chain genes. Further research is needed to clarify the relationship between oral CD30+ TLPDs and TUGSE.

创伤性溃疡性肉芽肿伴间质嗜酸性粒细胞增多:从反应性过程到低级别CD30 +淋巴细胞增生性疾病。
综述目的:创伤性溃疡性肉芽肿伴间质嗜酸性粒细胞增多(TUGSE)是一种罕见的口腔黏膜良性溃疡性病变,存在于成人和婴儿(Riga-Fede)中。本文将探讨TUGSE的临床表现、发病机制、组织病理学特征和治疗方法。本文简要讨论了口腔CD30+ t淋巴细胞增生性疾病(tlpd)及其与TUGSE病变的潜在关系。最近的发现:虽然传统上被认为是反应性的,但最近的一些证据表明,TUGSE可能与CD30+ t细胞淋巴增生性疾病(tlpd)有共同的特征,可能代表了一系列病变,从而使诊断和治疗方法复杂化。虽然一些TUGSE病例表现出CD30阳性和t细胞受体γ (TCRγ)链基因单克隆,但没有病例进展为广泛或全身性淋巴瘤。很少报道的口腔CD30+ tlpd与皮肤CD30+ tlpd具有相同的特征,表现出惰性的生物学行为和良好的预后,在切口活检后经常出现完全或部分消退。TUGSE表现为愈合缓慢的溃疡,边界凸起,硬化,通常影响舌头,可能模仿鳞状细胞癌。虽然创伤似乎是一个重要因素,但确切的发病机制尚不清楚。组织病理学上,病变表现为溃疡,多形态浸润,富含嗜酸性粒细胞,延伸至粘膜下层,伴有特征性肌纤维变性和不同类型的非典型单核细胞。病情通常遵循自我限制的过程,预后良好,对保守治疗反应良好。即使对于CD30+单克隆TCRγ链基因的病例,也可能不需要积极的治疗和广泛的随访。需要进一步的研究来阐明口服CD30+ tlpd与TUGSE之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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