Kanaan Hassan, Al-Maghrabi Jaudah, Linjawi Ayman, Al-Abbassi Amira, Dandan Abdelghani, Haider Abdul Razzaq
Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
Arch Pathol Lab Med. 2006 Feb;130(2):205-8. doi: 10.5858/2006-130-205-IDCSOT.
Interdigitating dendritic cell sarcoma is an extremely rare malignancy derived from antigen-presenting cells. Dendritic cells constitute a heterogeneous group of cells, which includes Langerhans cells, dermal dendrocytes, follicular dendritic cells, and interdigitating dendritic cells present in lymphoid and nonlymphoid organs. We report the case of a 36-year-old woman who presented with epigastric pain, projectile vomiting, and significant weight loss. Upper gastrointestinal endoscopy showed a duodenal lesion; a biopsy of the lesion was taken and was diagnosed as sarcoma. She underwent a Whipple procedure. A final diagnosis of interdigitating dendritic cell sarcoma was made, with liver and peripancreatic lymph node involvement. The patient deteriorated rapidly and died 4 months later. Although interdigitating dendritic cell sarcoma of the duodenum is extremely rare, we think it should be included in the differential diagnosis of unusual spindle cell tumors with a rich lymphocytic infiltrate.
交指状树突状细胞肉瘤是一种极其罕见的源自抗原呈递细胞的恶性肿瘤。树突状细胞构成了一组异质性细胞,其中包括朗格汉斯细胞、真皮树突状细胞、滤泡树突状细胞以及存在于淋巴器官和非淋巴器官中的交指状树突状细胞。我们报告了一例36岁女性患者,其表现为上腹部疼痛、喷射性呕吐和显著体重减轻。上消化道内镜检查显示十二指肠有病变;对病变进行活检,诊断为肉瘤。她接受了惠普尔手术。最终诊断为交指状树突状细胞肉瘤,伴有肝脏和胰周淋巴结受累。患者病情迅速恶化,4个月后死亡。尽管十二指肠交指状树突状细胞肉瘤极为罕见,但我们认为在诊断伴有丰富淋巴细胞浸润的不寻常梭形细胞瘤时应将其纳入鉴别诊断。