Monti Manlio, Limarzi Francesco, Oboldi Devil, Sbrancia Monica, Pallotti Maria Caterina, Miserocchi Giulia, Ghini Virginia, Zanuccoli Sofia, Cagnazzo Sara, Frassineti Giovanni Luca
Department of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Pathology Unit, "Morgagni-Pierantoni" Hospital, Forlì, Italy.
Front Oncol. 2024 Nov 20;14:1419923. doi: 10.3389/fonc.2024.1419923. eCollection 2024.
Primary squamous cell carcinoma (SCC) can originate in different parts of the body, including the head, neck, lung, bronchus, cervix uteri, esophagus, and cardia, and subsequently metastasize to the stomach. Primary gastric squamous cell carcinoma (GSCC) is a rare disease. To better understand GSCC, we present the case of a 72-year-old woman with a primary GSCC. A chest and abdominal CT scan highlighted a 36×26 mm mass with a 41 mm longitudinal diameter, which included the origin of the celiac tripod. The disease appeared to originate exophytically from the gastric wall. An ultrasound-endoscopy showed a hypoechoic formation with not well-defined margins measuring 40×30 mm involving the origin of the celiac tripod, about 10 mm from the gastric wall. An endoscopic fine-needle aspiration showed a poorly differentiated carcinoma. A PET/CT scan showed a hyperaccumulation of the known expansive formation at the celiac tripod (SUV 11.9) without specific cleavage planes from the stomach. A gastroscopy showed a regular esophagus and an absence of gastric protruding lesions. In the subcardial area, on the posterior wall, there was a slightly raised sub-centimetric area covered by bleeding mucosa where the biopsy had been performed. The pathological report showed chronic gastritis. An eco-endoscopy confirmed a hypoechoic neoformation measuring 30×40 mm that appeared to originate from the muscular layer of the gastric wall. The biopsy report was positive for broad-spectrum cytokeratins (AE1/AE3), CK5/6/7, p40, p63 and negative for CK20, PAS, TTF-1, anti-smooth muscle actin, CD45 (LCA), ERG, and S100. The clinical picture suggested poorly differentiated carcinoma with squamous differentiation. We analyzed the main classifications of GSCC cases and compared their characteristics. It is clear that to have an appropriate definition of GSCC, well-defined diagnostic criteria are needed. Currently, there is no consensus. For practical purposes, it would be better to include a panel of CK and p40 to distinguish GSCC from adenocarcinoma. A GSCC outside the mucosa is not rare and could be a true entity.
原发性鳞状细胞癌(SCC)可起源于身体的不同部位,包括头部、颈部、肺部、支气管、子宫颈、食管和贲门,随后转移至胃部。原发性胃鳞状细胞癌(GSCC)是一种罕见疾病。为了更好地了解GSCC,我们报告一例72岁原发性GSCC女性患者的病例。胸部和腹部CT扫描显示一个36×26 mm的肿块,纵径为41 mm,包括腹腔干起始部。病变似乎从胃壁向外生长。超声内镜显示一个边界不清的低回声结构,大小为40×30 mm,累及腹腔干起始部,距胃壁约10 mm。内镜细针穿刺显示为低分化癌。PET/CT扫描显示腹腔干处已知的扩张性病变有高摄取(SUV 11.9),与胃之间无明确分界平面。胃镜检查显示食管正常,无胃突出性病变。在心下区后壁,有一个略隆起的小于1厘米的区域,覆盖有出血黏膜,此处已进行活检。病理报告显示为慢性胃炎。超声内镜证实一个大小为30×40 mm的低回声新生物,似乎起源于胃壁肌层。活检报告显示广谱细胞角蛋白(AE1/AE3)、CK5/6/7、p40、p63阳性,CK20、PAS、TTF-1、抗平滑肌肌动蛋白、CD45(LCA)、ERG和S100阴性。临床表现提示为伴有鳞状分化的低分化癌。我们分析了GSCC病例的主要分类并比较了它们各自特征。显然,为对GSCC有一个恰当的定义,需要明确的诊断标准。目前尚无共识。出于实际目的,最好纳入一组细胞角蛋白和p40以区分GSCC与腺癌。黏膜外的GSCC并不罕见,可能是一种真正的实体。