Tamaki Ichiro, Hosoda Yohei, Sasano Hironobu, Sasaki Yu, Kiyochi Hidenori, Taki Yoshiro, Komoto Izumi
Department of Surgery, Kansai Electric Power Hospital, Fukushima 2-1-7, Fukushima-ku, Osaka City, Osaka, 553-0003, Japan.
Graduate School of Medicine, Anatomic Pathology, Tohoku University, Sendai, Japan.
Surg Case Rep. 2020 Nov 3;6(1):279. doi: 10.1186/s40792-020-01058-7.
Glomus tumors are subcutaneous tumors arising from glomus bodies, thermoregulatory components of the skin. These tumors could occur in visceral organs where glomus bodies are not normally present. Herein, we report a case of primary pancreatic glomus tumor with aggressive direct invasion into the superior mesenteric vein (SMV). To the best of our knowledge, this is the second case report of a glomus tumor arising in the pancreas.
A 46-year-old woman was referred to our hospital due to vomiting with epigastric and back pain. Dynamic-CT revealed a well-circumscribed hypervascular mass, measuring 37 mm in its maximal diameter involving the pancreatic head. Both CT and endoscopic ultrasonography (EUS) revealed direct invasion into the SMV and radiologically suspected tumor thrombus. Biopsy sample obtained by EUS-guided fine needle aspiration revealed proliferation of small cells, round-to-oval tumor cells with round nuclei and scant cytoplasm. A histological diagnosis of pancreatic neuroendocrine tumor, G1 was initially considered. Therefore, subtotal stomach-preserving pancreatoduodenectomy using Child-II reconstruction was subsequently performed. Her SMV was resected and reconstructed due to extensive tumor involvement. Subsequent histopathological analysis revealed solid tumor cells proliferation that comprised oval-shaped nuclei and scant cytoplasm around disorganized or slit-shaped vessels in hematoxylin-eosin-stained slides. Immunohistochemical analysis then demonstrated positive immunoreactivity for smooth muscle actin, vimentin, and CD34, but negative for chromogranin A, synaptophysin, CD56, and signal transducer and activator of transcription 6. Based on these histological findings of resected specimens, the lesion was subsequently diagnosed as a primary pancreatic glomus tumor harboring direct invasion into the SMV. Her postoperative course was uneventful and annual surveys for the following 4 years post-op detected no clinical signs of recurrence.
We report a very rare case of glomus tumor of the pancreas accompanied by venous invasion. Curative surgical resection is the best treatment option for pancreatic glomus tumors. Although pancreatic glomus tumor is rare, it should be taken into consideration in the differential diagnosis of a pancreatic solid tumor with hypervascularity.
血管球瘤是起源于血管球的皮下肿瘤,血管球是皮肤的体温调节成分。这些肿瘤可发生于正常情况下不存在血管球的内脏器官。在此,我们报告一例原发性胰腺血管球瘤伴直接侵犯肠系膜上静脉(SMV)的病例。据我们所知,这是第二例胰腺血管球瘤的病例报告。
一名46岁女性因呕吐伴上腹部和背部疼痛转诊至我院。动态CT显示一个边界清晰的高血运肿块,最大直径37mm,累及胰头。CT和内镜超声(EUS)均显示肿瘤直接侵犯SMV,影像学怀疑有肿瘤血栓形成。EUS引导下细针穿刺活检样本显示小细胞、圆形至椭圆形肿瘤细胞增生,细胞核圆形,胞质稀少。最初考虑为胰腺神经内分泌肿瘤G1级的组织学诊断。因此,随后进行了保留胃的Child-II式重建胰十二指肠次全切除术。由于肿瘤广泛累及,其SMV被切除并重建。随后的组织病理学分析显示,苏木精-伊红染色切片中,实体肿瘤细胞增生,细胞核呈椭圆形,围绕杂乱或裂隙状血管的胞质稀少。免疫组织化学分析显示平滑肌肌动蛋白、波形蛋白和CD34免疫反应阳性,但嗜铬粒蛋白A、突触素、CD56以及信号转导和转录激活因子6免疫反应阴性。基于切除标本的这些组织学发现,该病变随后被诊断为原发性胰腺血管球瘤伴直接侵犯SMV。她术后恢复顺利,术后4年的年度检查未发现复发的临床迹象。
我们报告了一例非常罕见的胰腺血管球瘤伴静脉侵犯的病例。根治性手术切除是胰腺血管球瘤的最佳治疗选择。尽管胰腺血管球瘤罕见,但在鉴别诊断具有高血运的胰腺实性肿瘤时应予以考虑。