儿童期双侧颌下腺慢性硬化性颌下腺炎--诊断难题。

IF 1.2 4区 医学 Q4 DEVELOPMENTAL BIOLOGY Romanian Journal of Morphology and Embryology Pub Date : 2024-01-01 DOI:10.47162/RJME.65.1.14
Octavian Marius Dincă, Alexandru Bucur, Sabina Andrada Zurac, Tiberiu Niţă, Gheorghiţă Jugulete, George Cristian Vlădan, Lavinia Cristina Pădurariu
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引用次数: 0

摘要

慢性硬化性颌下腺炎(CSS)目前被列入免疫球蛋白 G4(IgG4)相关疾病,是一种未得到充分认识的炎症性病变,多发于 40-60 岁成年人的颌下腺。据我们所知,迄今为止只有一例儿童颌下腺 CSS 病例。我们现在介绍一例 5 岁男童的 CSS 病例。他出现双侧颌下腺肿物,临床上类似于不连续的肿块,怀疑是肿瘤。完全切除的肿瘤主要由富含 IgG4 阳性细胞的致密淋巴浆细胞炎症浸润组成[每个高倍视野有 77-90 个 IgG(+) 细胞;IgG4(+)∕IgG(+) 细胞比为 42.77%]。我们讨论了该病例的特殊性,并回顾了有关 CSS 的文献。
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Chronic sclerosing sialadenitis of the bilateral submandibular glands in childhood - a diagnostic dilemma.

Chronic sclerosing sialadenitis (CSS), currently included in the group of immunoglobulin G4 (IgG4)-related diseases, is an under-recognized inflammatory lesion that afflicts mostly the submandibular gland of 40-60 years adults. To our knowledge, only one case of CSS located in the submandibular gland has been reported in childhood to date. We present a case of CSS in a 5-year-old male child. He presented with bilateral submandibular swellings that clinically resembled discrete lumps, suspected to be tumors. The completely resected tumors composed predominantly of dense lymphoplasmacytic inflammatory infiltrate rich in IgG4-positive cells [77-90 IgG(+) cells per high-power field; IgG4(+)∕IgG(+) cells ratio of 42.77%]. We discuss the peculiarities of this case, and we also review the literature on CSS.

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来源期刊
CiteScore
1.70
自引率
20.00%
发文量
221
审稿时长
3-8 weeks
期刊介绍: Romanian Journal of Morphology and Embryology (Rom J Morphol Embryol) publishes studies on all aspects of normal morphology and human comparative and experimental pathology. The Journal accepts only researches that utilize modern investigation methods (studies of anatomy, pathology, cytopathology, immunohistochemistry, histochemistry, immunology, morphometry, molecular and cellular biology, electronic microscopy, etc.).
期刊最新文献
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