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腹膜后间隙的 Castleman 病酷似椎旁神经鞘瘤:一例报告。

Castleman's disease in the retroperitoneal space mimicking a paraspinal schwannoma: a case report.

机构信息

Department of Orthopedic Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima-city, Kagoshima, 890-8520, Japan.

出版信息

World J Surg Oncol. 2013 May 23;11:108. doi: 10.1186/1477-7819-11-108.

Abstract

BACKGROUND

Castleman's disease is a rare disease characterized by lymph node hyperplasia. Its occurrence in the retroperitoneal space has rarely been reported, making its preoperative diagnosis difficult. Here, we report a case of retroperitoneal Castleman's disease, which radiologically resembled paraspinal schwannoma.

CASE PRESENTATION

A 33-year-old Japanese man with epigastric discomfort underwent abdominal ultrasonic examination revealing a solid mass next to the right kidney. Computed tomography demonstrated a well-circumscribed mass with central calcification in the right psoas muscle. Because the mass presented a dumbbell-like shape extending to the intervertebral foramen, neurogenic tumor was suspected. Both iodine-123 metaiodobenzylguanidine and gallium-67 scintigraphies were negative in the mass, whereas thallium-201 mildly accumulated in the tumor, suggesting blood flow to the tumor. Positron emission tomography revealed accumulation of fluorine-18-2-fluoro-2-deoxy-d-glucose in the tumor at a standard uptake value of 4.7, whereas no other abnormal uptake suggestive of metastatic lesion was noted. On the basis of imaging studies, we mostly suspected paraspinal schwannoma, although malignancy was not completely excluded. Angiography showed feeding vessels from the right lumbar arteries, which were embolized with porous gelatin particles in order to reduce intraoperative bleeding. Surgical resection was performed using a retroperitoneal approach, which revealed the tumor in the swollen psoas muscle. Intraoperative pathological examination of a frozen section revealed no evidence of malignancy; thus, marginal excision of the tumor was performed. The tumor adhered tightly to surrounding muscle tissues, resulting in 940 g of intraoperative blood loss. The pathological examination demonstrated infiltration of lymphocytes surrounding small germinal centers with extensive capillary proliferation. Immunostaining revealed that proliferated lymphocytes were CD3-negative and CD79a-positive.

CONCLUSIONS

Although a dumbbell-shaped mass in a paraspinal region is indicative of a schwannoma for orthopedic surgeons, the possibility of Castleman's disease should be considered if a central low-signal area in fissured and a radial pattern is detected on computed tomography or magnetic resonance imaging. Appropriate preparation for massive bleeding during the treatment of Castleman's disease, including angiography and embolization, would be helpful for performing surgical procedures safely.

摘要

背景

Castleman 病是一种罕见的疾病,其特征为淋巴结增生。其发生在腹膜后腔的情况很少被报道,导致术前诊断困难。在此,我们报告一例腹膜后 Castleman 病,其影像学上类似于椎旁神经鞘瘤。

病例介绍

一名 33 岁的日本男性,上腹不适,腹部超声检查发现右肾旁有一实性肿块。计算机断层扫描显示右腰肌内有一边界清楚的肿块,中央有钙化。由于肿块呈哑铃状延伸至椎间孔,故怀疑为神经源性肿瘤。肿块的碘-123 间碘苄胍和镓-67 闪烁显像均为阴性,而铊-201 则轻度积聚于肿瘤中,提示肿瘤有血流。正电子发射断层扫描显示氟-18-2-氟-2-脱氧-d-葡萄糖在肿瘤中的标准摄取值为 4.7,而无其他异常摄取提示转移性病变。基于影像学研究,我们主要怀疑椎旁神经鞘瘤,但不能完全排除恶性肿瘤。血管造影显示肿瘤有来自右腰动脉的供血血管,为减少术中出血,用多孔明胶颗粒进行了栓塞。采用腹膜后入路进行肿瘤切除,发现肿瘤位于肿胀的腰肌中。术中冷冻切片病理检查未见恶性证据,因此仅行肿瘤边缘切除。肿瘤与周围肌肉组织紧密粘连,术中失血 940 克。病理检查显示淋巴细胞浸润,围绕着广泛毛细血管增生的小生发中心。免疫组化染色显示增生的淋巴细胞 CD3 阴性,CD79a 阳性。

结论

尽管骨科医生认为椎旁区域的哑铃状肿块提示神经鞘瘤,但如果 CT 或磁共振成像显示有裂隙状中央低信号区和放射状模式,则应考虑 Castleman 病的可能性。在治疗 Castleman 病时,包括血管造影和栓塞,适当准备大出血的情况将有助于安全地进行手术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6452/3663832/e6bae6cfb4a8/1477-7819-11-108-1.jpg

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