Department of Gynecology and Obstetrics, The First Affiliated Hospital of Jinan University Guangzhou, Guangzhou, 510630, Guangdong, People's Republic of China.
Department of Pathology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, People's Republic of China.
BMC Pregnancy Childbirth. 2023 Jul 20;23(1):528. doi: 10.1186/s12884-023-05849-2.
Endodermal sinus tumor (EST) is a malignant tumor originating from the ovary or testis. In most case, ultrasound examination shows ovarian mass. But there is a special kind of extra-gonadal endodermal sinus tumor, which occur in organs other than gonads with insidious onset. Here we reported a case of endodermal sinus tumor, which originated from the sacral ligament presenting as an acute lower abdominal pain.
A 14-year-old girl was admitted to the hospital because of acute lower abdominal pain. The ultrasound showed a mass with 72 mm × 64 mm × 50 mm in Douglas, and there was no abnormality in bilateral ovaries and fallopian tubes. Laparoscopic exploration showed a large amount of blood clots in the pelvic cavity. After removal of the blood, we found rotten fish-like tissue in the left sacral ligament, rapid pathology suggested endodermal sinus tumor. After the operation, we retrospectively examined the value of alpha-fetoprotein (AFP), which was found to be elevated, and post-operative paraffin pathology confirmed the diagnosis. After four cycles of BEP chemotherapy, exploratory laparotomy was performed to remove the visible lesion, but postoperative pathology showed no abnormality. At the one-year follow-up, the patient remained recurrence-free.
Extra-gonadal germ cell tumors are rarely reported. When young teenagers complain of acute lower abdominal pain with elevated AFP, but there was no lesion in bilateral ovaries and fallopian tubes, we must think about the possibility of endodermal sinus tumors. Accurate diagnosis facilitates complete resection of lesions and improves patient's outcomes.
内胚窦瘤(EST)是一种起源于卵巢或睾丸的恶性肿瘤。大多数情况下,超声检查显示卵巢肿块。但有一种特殊的卵巢外内胚窦瘤,其发生在除性腺以外的器官,起病隐匿。本文报道了一例起源于骶韧带的内胚窦瘤,表现为急性下腹痛。
一名 14 岁女孩因急性下腹痛入院。超声显示 Douglas 处有一 72mm×64mm×50mm 的肿块,双侧卵巢和输卵管无异常。腹腔镜探查见盆腔内有大量血凝块,清除血液后,我们发现左侧骶韧带有腐烂的鱼肉样组织,快速病理提示为内胚窦瘤。术后回顾性检查甲胎蛋白(AFP)值,发现升高,术后石蜡病理证实诊断。行 BEP 化疗 4 周期后,行剖腹探查术以切除可见病灶,但术后病理未见异常。在一年的随访中,患者无复发。
性腺外生殖细胞肿瘤罕见。当年轻青少年出现急性下腹痛伴 AFP 升高,但双侧卵巢和输卵管无病变时,必须考虑内胚窦瘤的可能性。准确的诊断有助于彻底切除病灶,改善患者的预后。