Watanabe Yukihiro, Okamoto Kojun, Okada Katsuya, Aikawa Masayasu, Koyama Isamu, Yamaguchi Hiroshi
Department of Gastroenterological Surgery, Saitama Medical University International Medical Center, Yamane 1397-1, Hidaka, Saitama, Japan.
Department of Pathology, Saitama Medical University International Medical Center, Yamane 1397-1, Hidaka, Saitama, Japan.
Pathol Int. 2017 Apr;67(4):202-207. doi: 10.1111/pin.12516. Epub 2017 Feb 16.
Solid pseudopapillary neoplasms (SPNs) may have an aggressive clinical course, but clinical predictors of this condition have not been thoroughly evaluated. We performed a retrospective study of 11 cases of SPN managed in our hospital between January 2007 and April 2015. Of these 11 cases, we encountered a single case with an aggressive clinical course. Histological, immunohistochemical, and clinical features were compared to identify predictors of poor prognosis. The 11 patients comprised four women and seven men with a median age of 41 years (range, 26-58 years). Clinical symptoms were nonspecific and the median tumor size was 4.6 cm (range, 1.4-18 cm). The patient with an aggressive clinical course developed multiple liver metastases within three months and died seven months after surgery. Pathological features of the tumor in this case included lymph node metastases, a diffuse growth pattern, extensive tumor necrosis, high mitotic rate, and immunohistochemistry. These features were not observed in patients who survived without recurrence at a median follow-up of 25 months (range, 6-82 months). Characteristic pathological features and a high proliferative index, as assessed by Ki-67 staining, may predict poor outcome in cases of SPN.
实性假乳头状肿瘤(SPN)可能具有侵袭性的临床病程,但该疾病的临床预测因素尚未得到充分评估。我们对2007年1月至2015年4月期间在我院接受治疗的11例SPN患者进行了一项回顾性研究。在这11例患者中,我们遇到了1例具有侵袭性临床病程的病例。对其组织学、免疫组化和临床特征进行比较,以确定预后不良的预测因素。11例患者包括4名女性和7名男性,中位年龄为41岁(范围26 - 58岁)。临床症状不具特异性,肿瘤中位大小为4.6 cm(范围1.4 - 18 cm)。具有侵袭性临床病程的患者在三个月内出现多发肝转移,并在手术后七个月死亡。该病例肿瘤的病理特征包括淋巴结转移、弥漫性生长模式、广泛的肿瘤坏死、高有丝分裂率以及免疫组化表现。在中位随访25个月(范围6 - 82个月)未复发存活的患者中未观察到这些特征。通过Ki - 67染色评估的特征性病理特征和高增殖指数可能预示SPN病例的不良预后。