扁桃体利什曼病:一种罕见的模拟口咽恶性肿瘤的临床实体-来自意大利东北部的病例系列。

IF 3.2 Q2 PATHOLOGY
Giulia Querzoli, Margherita Ortalli, Stefania Varani, Matteo Errani, Andrea Ambrosini-Spaltro, Marina Del Vecchio, Anna Rita Lombardi, Paolo Rinaldi, Carlo Biagetti, Riccardo Albertini, Luca Amorosa, Alessandro Rosti, Marco Trebbi, Paolo Farneti, Ernesto Pasquini, Antonio Mastroianni, Maria Pia Foschini, Valeria Gaspari
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引用次数: 0

摘要

目的:基底利什曼病(TL)在欧洲是一种被忽视的疾病,由于其多变的临床表现,经常被漏诊或误诊。粘膜利什曼病(ML)是TL的一种罕见表现,孤立的扁桃体利什曼病是一种更罕见的发现,报道的病例很少。本研究旨在通过描述意大利东北部艾米利亚-罗马涅地区(ERR)诊断出的5例孤立扁桃体利什曼病,扩大对这一不寻常临床实体的认识,强调诊断挑战和治疗结果。方法:2014年1月至2024年12月,在ERR医院耳鼻喉科对所有连续出现单侧扁桃体肿胀和咽痛的患者进行评估。转诊医院进行组织病理学分析、特殊染色(H&E、Giemsa、PAS、Ziehl-Neelsen)和免疫染色(CD1a)。针对利什曼原虫kDNA和rRNA进行实时PCR鉴定。根据目前的TL指南进行治疗。结果:我们纳入了5例患者,他们表现为单侧扁桃体肿胀,类似恶性肿瘤,组织学诊断为非坏死性肉芽肿。组织学显示4例为无纺体。聚合酶链反应证实所有病例感染利什曼原虫。用两性霉素B或喷他脒脂质体治疗导致临床完全缓解。结论:在头颈部肿瘤的鉴别诊断中应考虑孤立体利什曼病,特别是在流行地区。组织学和分子工具对于准确诊断至关重要。提高认识的临床医生和病理学家是必要的,以提高认识和管理这种罕见的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tonsillar Leishmaniasis: A Rare Clinical Entity Mimicking Malignancy in the Oropharynx - A Case Series from Northeastern Italy.

Purpose: Tegumentary leishmaniasis (TL) is a neglected disease in Europe, often underdiagnosed or misdiagnosed due to its variable clinical presentation. Mucosal leishmaniasis (ML) is a rare manifestation of TL, and isolated tonsillar leishmaniasis is an even rarer finding, with very few reported cases. This study aims to expand knowledge on this unusual clinical entity by describing five cases of isolated tonsillar leishmaniasis diagnosed in the Emilia-Romagna region (ERR), northeastern Italy, emphasizing diagnostic challenges and treatment outcomes.

Methods: Between January 2014 and December 2024, all consecutive patients presenting with unilateral tonsillar swelling and pharyngodynia were evaluated at otolaryngology units in ERR hospitals. Histopathological analysis, special stains (H&E, Giemsa, PAS, Ziehl-Neelsen), and immunostaining (CD1a) were performed at the referring hospital. Microbiological confirmation was obtained through real-time PCR targeting Leishmania kDNA and rRNA. Treatment was administered according to current TL guidelines.

Results: We included five patients who presented with unilateral tonsillar swelling mimicking malignancy and with a histological diagnosis of non-necrotizing granulomas. Histology revealed amastigotes in four cases. PCR confirmed Leishmania infection in all cases. Treatment with liposomal amphotericin B or pentamidine led to complete clinical remission.

Conclusion: Isolated tonsillar leishmaniasis should be considered in the differential diagnosis of head and neck tumors, especially in endemic regions. Histological and molecular tools are essential for accurate diagnosis. Increased awareness among clinicians and pathologists is necessary to improve recognition and management of this rare presentation.

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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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