Myofibroblastic proliferation of the tongue with significant differential diagnosis - a case report and review of literature

IF 2 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Dr. Ioana Ghita , Dr. Christopher Fielding , Dr. Joshua Lubek , Dr. Rania Younis
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引用次数: 0

Abstract

Lesions of Myofibroblastic origin are very rare to occur in the tongue, sometimes they have an aggressive presentation that could be easily misdiagnosed as malignancy. There is not a clear etiology, however trauma and infection are suggested factors. Histologically, myofibroblastic and inflammatory cells are present.

Here we present a case report of a 46-year-old Caucasian female that presented with approximately three year-history of laceration of dorsum tongue that was recently further traumatized by biting it. The clinical exam revealed a traumatic raised nodular lesion on the right side towards the mid-line of dorsum tongue.

The histological findings revealed a poorly demarcated mass of atypical proliferating spindle cells, infiltrating into the muscle fibers and extending to the base of the specimen. Desmin and Myogenin, were focally positive in regenerating/degenerating muscle cells. MSA was diffusely positive in the spindle cells. Within the submucosa there was a proliferation of actin positive myofibroblasts with associated inflamed granulation tissue containing scattered acute and chronic inflammatory cells. CK (AE1/AE3), CD31, S-100, and HMB45 were negative for the spindle cells. CD31 highlighted the small blood vessels in the granulation tissue. Perivascular necrosis was noted. Ki-67 showed high proliferative index (>25%). Factor XIIIa highlighted fibroblasts and MyoD1 showed scattered positivity.

The final diagnosis was in favor of a benign reactive myofibroblastic proliferation.

Myofibroblastic proliferation lesion is a challenging diagnosis because of the clinical appearance and the histological features mimicking malignancy. For this reason, it is imperative to have an accurate diagnosis to prevent unnecessary radical treatment.

舌肌纤维细胞增生与重要鉴别诊断--病例报告和文献综述
肌纤维母细胞源性病变发生在舌头上非常罕见,有时表现为侵袭性,很容易被误诊为恶性肿瘤。目前还没有明确的病因,但创伤和感染是可能的因素。组织学上,存在肌成纤维细胞和炎症细胞。我们在此报告一例 46 岁白种女性的病例,她的舌背有约 3 年的撕裂史,最近因咬伤舌背而进一步受创。组织学检查结果显示,这是一个界限不清的非典型增生纺锤形细胞肿块,浸润到肌纤维中并延伸到标本的基底。Desmin和Myogenin在再生/变性肌肉细胞中呈点状阳性。纺锤细胞中的 MSA 呈弥漫性阳性。在粘膜下层,肌动蛋白阳性的肌成纤维细胞增生,伴有炎性肉芽组织,其中含有散在的急性和慢性炎症细胞。纺锤细胞的 CK(AE1/AE3)、CD31、S-100 和 HMB45 均为阴性。肉芽组织中的小血管突出显示为 CD31。可见血管周围坏死。Ki-67 显示增殖指数较高(25%)。肌成纤维细胞增生病变是一种具有挑战性的诊断,因为其临床表现和组织学特征与恶性肿瘤相似。由于临床表现和组织学特征酷似恶性肿瘤,因此肌成纤维细胞增生病变的诊断具有挑战性,必须做出准确诊断,以避免不必要的根治性治疗。
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来源期刊
Oral Surgery Oral Medicine Oral Pathology Oral Radiology
Oral Surgery Oral Medicine Oral Pathology Oral Radiology DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.80
自引率
6.90%
发文量
1217
审稿时长
2-4 weeks
期刊介绍: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology is required reading for anyone in the fields of oral surgery, oral medicine, oral pathology, oral radiology or advanced general practice dentistry. It is the only major dental journal that provides a practical and complete overview of the medical and surgical techniques of dental practice in four areas. Topics covered include such current issues as dental implants, treatment of HIV-infected patients, and evaluation and treatment of TMJ disorders. The official publication for nine societies, the Journal is recommended for initial purchase in the Brandon Hill study, Selected List of Books and Journals for the Small Medical Library.
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