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孤立性髓外浆细胞瘤表现为无症状的腭红斑:病例报告。

Solitary Extramedullary Plasmacytoma Presenting as Asymptomatic Palatal Erythroplakia: Report of a Case.

机构信息

Otorhinolaryngology-Head & Neck Surgery Department, San Raffaele Hospital, University Vita-Salute, 20132 Milan, Italy.

School of Medicine, Vita-Salute San Raffaele University, 20132 Milan, Italy.

出版信息

Int J Environ Res Public Health. 2021 Apr 4;18(7):3762. doi: 10.3390/ijerph18073762.

Abstract

Solitary plasmacytoma (SP) is a rare malignant tumor of plasma cells with no systemic spread; however, when it disseminates and affects multiple skeletal sites, it is called multiple myeloma (MM). The etiology of solitary plasmacytoma is unknown, with two possible subtypes: solitary extramedullary plasmacytoma (EMP) and solitary bone plasmacytoma (SBP). We present a case of EMP arising as asymptomatic erythroplakia of the palate, which is rarely described in the literature. The definitive diagnosis was obtained with immunohistochemical studies, after which the lesion was subjected to excisional biopsy. At present, after two years of close follow-up, the patient has shown no signs of relapse or conversion to MM. The uniqueness of the case highlights the possibility of an atypical EMP lesion in the head and neck, thus posing a diagnostic and therapeutic challenge for physicians.

摘要

孤立性浆细胞瘤(SP)是一种罕见的浆细胞恶性肿瘤,无全身播散;然而,当它播散并影响多个骨骼部位时,就称为多发性骨髓瘤(MM)。孤立性浆细胞瘤的病因尚不清楚,可能有两种亚型:孤立性髓外浆细胞瘤(EMP)和孤立性骨浆细胞瘤(SBP)。我们报告了一例发生于无症状硬腭红细胞增多症的 EMP 病例,这在文献中很少描述。通过免疫组织化学研究获得明确诊断,然后对病变进行切除活检。目前,经过两年的密切随访,患者未出现复发或转化为 MM 的迹象。该病例的独特性强调了头颈部可能存在非典型 EMP 病变,从而对医生的诊断和治疗提出了挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9831/8038516/b3f0882729fc/ijerph-18-03762-g001.jpg

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