Miettinen Markku, Lasota Jerzy
Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Semin Diagn Pathol. 2006 May;23(2):70-83. doi: 10.1053/j.semdp.2006.09.001.
Gastrointestinal (GI) stromal tumors (GISTs) are the most common mesenchymal tumors specific to the GI tract, generally defined as KIT (CD117)-positive tumors with a characteristic set of histologic features. These tumors, derived from Cajal cells or their precursors, most commonly occur at the age >50 years in the stomach (60%), jejunum and ileum (30%), duodenum (4-5%), rectum (4%), colon and appendix (1-2%), and esophagus (<1%), and rarely as apparent primary extragastrointestinal tumors in the vicinity of stomach or intestines. Their overall incidence has been estimated as 10 to 20 per million, including incidental minimal tumors. GISTs are rare in children (<1%) and almost exclusively occur in stomach. They are common in patients with neurofibromatosis 1, who have a predisposition to (multiple) small intestinal GISTs. GISTs contain a spectrum from minute indolent tumors to sarcomas at all sites of occurrence. Their gross patterns are diverse, including nodular, cystic, and diverticular tumors. External involvement of pancreas and liver can simulate primary tumor in these organs. In general, gastric tumors have a more favorable prognosis than the intestinal ones with similar parameters. Gastric GISTs < or =10 cm and < or =5 mitoses per 50 HPFs have a low risk for metastasis, whereas those with >5 per 50 HPFs and >5 cm in diameter have a high risk for metastasis. In contrast, all intestinal GISTs >5 cm independent of mitotic rate have at least moderate risk for metastases, and all >5 mitoses per 50 HPFs have a high risk for metastases. Intestinal GISTs < or =5 cm with < or =5 mitoses per 50 HPFs have a low risk for metastases. Gastric GISTs can be divided into histologic subgroups including 4 spindle cell and 4 epithelioid variants. Intestinal GISTs are a histologically more homogeneous group and often contain distinctive extracellular collagen globules, skeinoid fibers. Immunohistochemical demonstration of KIT, CD34, or protein kinase theta positivity helps to properly identify these tumors.
胃肠道(GI)间质瘤(GISTs)是胃肠道特有的最常见的间充质肿瘤,通常定义为具有一组特征性组织学特征的KIT(CD117)阳性肿瘤。这些肿瘤起源于 Cajal 细胞或其前体,最常见于年龄>50岁的人群,其中胃(60%)、空肠和回肠(30%)、十二指肠(4-5%)、直肠(4%)、结肠和阑尾(1-2%)以及食管(<1%)较为常见,很少表现为胃或肠道附近明显的原发性胃肠道外肿瘤。其总体发病率估计为每百万人口中有10至20例,包括偶然发现的微小肿瘤。GISTs在儿童中罕见(<1%),几乎仅发生于胃。它们在1型神经纤维瘤病患者中常见,这些患者易患(多发)小肠GISTs。GISTs在所有发生部位都包含从微小惰性肿瘤到肉瘤的一系列病变。其大体形态多样,包括结节状、囊性和憩室状肿瘤。胰腺和肝脏的外部受累可能会模拟这些器官的原发性肿瘤。一般来说,具有相似参数的胃肿瘤比肠道肿瘤预后更好。直径≤10 cm且每50个高倍视野(HPFs)有丝分裂数≤5个的胃GISTs转移风险低,而每50个HPFs有丝分裂数>5个且直径>5 cm的胃GISTs转移风险高。相比之下,所有直径>5 cm的肠道GISTs,无论有丝分裂率如何,至少有中度转移风险,而每50个HPFs有丝分裂数>5个的所有肠道GISTs转移风险高。直径≤5 cm且每50个HPFs有丝分裂数≤5个的肠道GISTs转移风险低。胃GISTs可分为组织学亚组,包括4种梭形细胞和4种上皮样变体。肠道GISTs在组织学上是一个更均匀的群体,通常含有独特的细胞外胶原球和束状纤维。KIT、CD34或蛋白激酶θ阳性的免疫组织化学证明有助于正确识别这些肿瘤。