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下颌骨原发性骨内鳞状细胞癌:1例罕见且具挑战性的病例

Primary Intraosseous Squamous Cell Carcinoma of the Mandible: A Rare and Challenging Case.

作者信息

Byakodi Sanjay, Khan Mushtak, Nilkanthrao Pol Jaydeep, Kadkol Girish Anandrao, Purohit Gautam, Agiwal Devesh

机构信息

Department of Oral and Maxillofacial Surgery, Bharati Vidyapeeth (Deemed to be University) Dental College and Hospital, Sangli, IND.

Department of Surgical Pathology, Mahatma Gandhi Cancer Hospital, Miraj, IND.

出版信息

Cureus. 2025 Jun 10;17(6):e85690. doi: 10.7759/cureus.85690. eCollection 2025 Jun.

Abstract

Primary intraosseous squamous cell carcinoma (PIOSCC) is a rare cancer that arises within the jaws, often linked to odontogenic cysts or tumors. Its prevalence is about 1-2.5% of all odontogenic tumors and presents a diagnostic challenge due to its similarity to other jaw lesions. A 46-year-old woman complained of persistent pain in the left back region of the lower jaw, numbness over the left side of the lower lip, and reduced mouth opening. The doctor revised the initial diagnosis of periapical infection due to ongoing symptoms and a non-healing socket. Radiological imaging revealed an osteolytic lesion in the left ramus of the mandible, prompting further investigation. A biopsy confirmed the diagnosis of IOSCC following histopathological examination after segmental mandibulectomy. The final diagnosis was primary intraosseous well-differentiated squamous cell carcinoma of the left mandible. PIOSCC, even though it is uncommon, should be included in the list of possible diagnoses for jaw problems, especially those that have unclear, bone-destroying X-ray features. Symptoms such as pain, swelling, and sensory disturbances, along with radiologic findings, may suggest a malignant odontogenic tumor. Histological evaluation is crucial for differentiation from other odontogenic tumors, including ameloblastic carcinoma. Radical surgery, often combined with neck dissection, is the management of choice. Postoperative radiotherapy or chemotherapy may be considered, though their role remains unclear. The five-year survival rate with PIOSCC ranges from 30% to 46%, indicating a typically dismal prognosis. PIOSCC is an uncommon, aggressive tumor with a poor prognosis. Early diagnosis and accurate histopathological examination are essential to differentiate it from other odontogenic carcinomas and improve patient outcomes.

摘要

原发性骨内鳞状细胞癌(PIOSCC)是一种罕见的癌症,发生于颌骨内,常与牙源性囊肿或肿瘤相关。其发病率约占所有牙源性肿瘤的1%-2.5%,由于与其他颌骨病变相似,给诊断带来了挑战。一名46岁女性主诉下颌左后区域持续疼痛、下唇左侧麻木以及张口受限。由于症状持续且拔牙创不愈合,医生修正了最初根尖感染的诊断。影像学检查显示下颌骨左支有溶骨性病变,促使进一步检查。在进行节段性下颌骨切除术后,经组织病理学检查,活检确诊为IOSCC。最终诊断为左下颌原发性骨内高分化鳞状细胞癌。PIOSCC尽管不常见,但应列入颌骨问题可能的诊断清单中,尤其是那些具有不明确的、骨质破坏的X线特征的病例。疼痛、肿胀和感觉障碍等症状,以及影像学表现,可能提示恶性牙源性肿瘤。组织学评估对于与其他牙源性肿瘤,包括成釉细胞癌进行鉴别至关重要。根治性手术,通常联合颈部清扫术,是首选的治疗方法。术后可考虑放疗或化疗,但其作用仍不明确。PIOSCC的五年生存率为30%至46%,表明预后通常不佳。PIOSCC是一种罕见的侵袭性肿瘤,预后不良。早期诊断和准确的组织病理学检查对于将其与其他牙源性癌进行鉴别并改善患者预后至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6753/12243677/14d061424eb0/cureus-0017-00000085690-i01.jpg

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