An Uncommon Malignant Suprarenal Mesenchymal Tumor

IF 0.8 Q4 UROLOGY & NEPHROLOGY Indian Journal of Nephrology Pub Date : 2023-11-06 DOI:10.4103/ijn.ijn_278_23
None Prachi, Hema M. Aiyer, Gaurav Sharma
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Abstract

Dear Editor, Primary adrenal leiomyosarcoma is arare malignant tumor. Metastatic adrenal leiomyosarcoma and extension from the retroperitoneum are more frequent. Leiomyosarcoma occurs primarily in the myometrium, retroperitoneum, and soft tissues of the extremities. Herein we report a case in a 31 year old female who presented with abdominal pain. Contrast-enhanced computed tomography (CECT) and contrast-enhanced magnetic resonance imaging (CEMRI) abdomen revealed a large heterogeneously enhancing mass in the right suprarenal region abutting the surrounding structures such as liver, superior pole of right kidney, adjacent inferior vena cava, second part of duodenum, and right renal vein, causing its upliftment [Figure 1a]. Further, she underwent resection of the mass along with right nephrectomy. Pathological findings revealed a nonencapsulated mass measuring 8.5 × 5.5 × 4.5 cm. Cut surface appeared fleshy with hemorrhagic and necrotic areas [Figure 1b]. Microscopically, solid pattern of spindle cells showing marked pleomorphism with 30% areas of necrosis and 10–12 muscle fibers/10 high power fields, with compressed adrenal gland at the periphery was seen [Figure 1c]. Immunohistochemically, intense positivity for desmin, smooth muscle actin [Figure 1d], caldesmon, and vimentin was observed. Considering the aforementioned features, a diagnosis of conventional primary leiomyosarcoma of the adrenal gland, FNCLCC Grade 2 was rendered. After 15 months of follow-up, the patient remained free of recurrence. Adrenal leiomyosarcomas are rare tumors, usually diagnosed at an advanced stage due to nonspecificity of symptoms, contributing to poor prognosis. The gold standard for treatment is surgical excision, followed by chemotherapy and radiotherapy.Figure 1: Images of Primary adrenal leiomyosarcoma. (a) Imaging showing a large heterogeneously enhancing mass in the right suprarenal region abutting the surrounding structures. (b) Gross photograph of right nephrectomy specimen with a well defined fleshy suprarenal mass. (c) Microphotograph showing solid pattern of spindle cells showing marked pleomorphism and focal necrosis (H and E X100). (d) Immunoreactivity for Smooth Muscle actin (IHC stain for SMA X400)Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.
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一种罕见的肾上间质恶性肿瘤
原发性肾上腺平滑肌肉瘤是一种罕见的恶性肿瘤。转移性肾上腺平滑肌肉瘤和从腹膜后扩散更为常见。平滑肌肉瘤主要发生于四肢的肌层、腹膜后和软组织。在此,我们报告一例31岁女性腹痛。腹部对比增强计算机断层扫描(CECT)和增强磁共振成像(CEMRI)显示右侧肾上区有一个巨大的非均匀增强肿块,邻近周围结构,如肝脏、右肾上极、邻近下腔静脉、十二指肠第二部分和右肾静脉,导致其隆起[图1a]。此外,她接受了肿块切除术和右肾切除术。病理示8.5 × 5.5 × 4.5 cm无包被肿块。切口表面呈肉质,有出血和坏死区域[图1b]。显微镜下,纺锤体细胞呈实心形态,具有明显的多形性,30%坏死区域,10 - 12条肌纤维/10个高倍视场,外围肾上腺受压[图1c]。免疫组化结果显示,大蛋白、平滑肌肌动蛋白(Figure 1d)、caldesmon和vimentin呈强烈阳性。考虑到上述特征,诊断为常规原发性肾上腺平滑肌肉瘤,FNCLCC 2级。随访15个月后,患者无复发。肾上腺平滑肌肉瘤是一种罕见的肿瘤,由于症状不特异性,通常在晚期诊断,预后较差。治疗的金标准是手术切除,然后是化疗和放疗。图1:原发性肾上腺平滑肌肉瘤的图像。(a)影像学显示右侧肾上腺上区有一大块不均质增强肿块,邻近周围结构。(b)右侧肾切除术标本大体照片,可见清晰的肾上肉质肿块。(c)显微照片显示梭形细胞实心形态,显示明显的多形性和局灶性坏死(H和E X100)。(d)平滑肌肌动蛋白的免疫反应性(SMA X400的IHC染色)患者同意声明作者证明他们已经获得了所有适当的患者同意表格。财政支持及赞助无。利益冲突没有利益冲突。
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来源期刊
Indian Journal of Nephrology
Indian Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
1.40
自引率
0.00%
发文量
128
审稿时长
24 weeks
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