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肾细胞癌伴肉瘤样分化的诊断与管理挑战:一例报告

Challenges in the Diagnosis and Management of Renal Cell Carcinoma With Sarcomatoid Differentiation: A Case Report.

作者信息

Ehsan Evan, Ansari Ali Z, Hafeez Sahar, Patibandla Srihita, Beauti Samer M, Bhatt Nilay

机构信息

Department of Emergency Medicine, William Carey University College of Osteopathic Medicine, Hattiesburg, USA.

Department of Pathology, William Carey University College of Osteopathic Medicine, Hattiesburg, USA.

出版信息

Cureus. 2024 Nov 11;16(11):e73436. doi: 10.7759/cureus.73436. eCollection 2024 Nov.

Abstract

Metastatic sarcomatoid renal cell carcinoma (sRCC) is a significant therapeutic and diagnostic challenge due to its rarity and aggressiveness, which contribute to its poor prognosis. This case report presents the case of a 47-year-old Caucasian man with shortness of breath and right-sided abdominal pain. History revealed an extensive smoking history, a left renal mass diagnosed two months ago with inconclusive results, and an enlarged mass on computed tomography (CT) scan one week ago in an emergency department (ED) visit that showed signs consistent with metastatic disease. CT scan on presentation revealed a right posterolateral chest wall mass measuring 8.5×3.5 cm between the 10th and 11th ribs, as well as multiple bilateral pulmonary metastases. CT scan of the head revealed a soft tissue mass anterior to the epiglottis within the vallecula. Left renal pole mass was also consistent with neoplasm, with stable surrounding mass-like densities consistent with adenopathy and involvement of the adrenal gland. Histopathological examination of the 11 cm right chest wall mass biopsy revealed sRCC due to the visualization of spindle to epithelioid tumor with focal clear cell morphology and a prominent vascular network leading to a nested appearance. Management of his symptoms included thoracocentesis of the pleural effusion, nasal cannula due to low partial pressure of oxygen (PO2), pleurodesis, and trending down of the hypercalcemia. Oncology confirmed the spindle cell neoplasm due to stage IV renal cancer; the patient was transferred to hematology-oncology for further evaluation, but soon after succumbed to the complexities of metastatic disease. This case highlights the challenges of the management and diagnosis of metastatic sRCC over a three-week inpatient service, ultimately revealing a poor prognosis due to the aggressiveness and time of diagnosis, emphasizing the need for early detection methods and personalized treatment strategies. Further research is needed to explore novel therapeutic approaches to tackle this rare and aggressive variant of RCC.

摘要

转移性肉瘤样肾细胞癌(sRCC)因其罕见性和侵袭性而成为重大的治疗和诊断挑战,这导致其预后不良。本病例报告介绍了一名47岁白种男性,有呼吸急促和右侧腹痛症状。病史显示其有广泛的吸烟史,两个月前诊断出左肾肿块但结果不明确,一周前在急诊科就诊时计算机断层扫描(CT)显示肿块增大,提示有转移疾病迹象。初诊时的CT扫描显示右后外侧胸壁有一个位于第10和第11肋骨之间、大小为8.5×3.5 cm的肿块,以及双侧多发肺转移。头部CT扫描显示会厌谷内会厌前方有一个软组织肿块。左肾极肿块也与肿瘤相符,周围有稳定的肿块样密度,提示有淋巴结病和肾上腺受累。对11 cm的右胸壁肿块活检进行组织病理学检查,由于可见梭形到上皮样肿瘤,伴有局灶性透明细胞形态和突出的血管网络,呈巢状外观,确诊为sRCC。其症状的处理包括胸腔穿刺抽液、因低氧分压(PO2)给予鼻导管吸氧、胸膜固定术以及使高钙血症逐渐缓解。肿瘤学诊断因IV期肾癌确诊为梭形细胞瘤;患者被转至血液肿瘤科进一步评估,但不久后因转移性疾病的复杂性死亡。本病例突出了在为期三周的住院治疗期间转移性sRCC管理和诊断的挑战,最终因疾病的侵袭性和诊断时间而显示出预后不良,强调了早期检测方法和个性化治疗策略的必要性。需要进一步研究以探索新的治疗方法来应对这种罕见且侵袭性强的肾细胞癌变体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6aa5/11634550/1af7e463e478/cureus-0016-00000073436-i01.jpg

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