- Case report
- Open Access
A type of neoplasia deadlier than gastric adenocarcinoma? Report of a case of primary gastric squamous cell carcinoma
World Journal of Surgical Oncology volume 17, Article number: 113 (2019)
Primary gastric squamous cell carcinoma is an extremely rare malignancy with few case reports reported so far in the current medical literature. Its incidence varies between 0.04 and 0.07% of all gastric malignancies with a male predominance in the sixth decade of life. It has been found that this type of malignancy has a more aggressive behavior and associated poorer prognosis, when compared to gastric adenocarcinoma. Thus, the most appropriate management of this kind of neoplasia is still debatable due to the small number of reported cases.
We report the case of a 66-year-old man who underwent total gastrectomy with D2 lymphadenectomy for an ulcerative lesion in the fundus of the stomach that turned out to be primary gastric squamous cell carcinoma.
Upon confirmation of this specific malignancy, the affected patients should be enrolled in strict follow-up protocols after curative surgery, since the risk for metastasis is high. Physicians should maintain high clinical suspicion in order to diagnose these tumors at an early stage, along with the need to rule out any other possible primary sites of squamous malignancy.
Primary gastric squamous cell carcinoma (SCC) is an extremely rare entity with less than 100 cases described in the current medical literature. It represents 0.04–0.07% of all gastric cancers with an incidence ratio of men to women of about 5:1. The most common tumor location is the upper third of the stomach, and the prevalence is higher in the sixth decade of life. However, a wide spectrum of ages affected has been reported . The exact pathogenesis of primary gastric SCC is still unknown, but it seems to be more aggressive and prone to lymphovascular invasion compared to adenocarcinoma. The prognosis and the management of these uncommon tumors still remain unknown due to the low incidence of gastric SCCs. We describe a case of a 66-year-old man who was diagnosed with primary SCC of the fundus of the stomach. He underwent curative resection with total gastrectomy and D2 lymphadenectomy, but, due to the advanced stage of his disease, 2 months after the operation metastases to the lungs were apparent and adjuvant chemotherapy was initiated.
A 66-year-old man was referred to our surgical outpatient clinic because of an endoscopic report that was indicative of a small irregular ulcerative lesion in the fundus of the stomach. The histopathological report was consistent with gastric squamous carcinoma (AE1/AE3+, p40+, Chromogranin A−, Synaptophysin−, c-erB-2/HER2−). The patient complained of epigastric pain and abdominal cramps for the last 2 months with no incident of hematemesis, melena, or hematochezia. He had an unintentional weight loss of approximately 10 kg during the last 4 months. He was suffering from type 2 diabetes with a past medical history of smoking, 100 packs per year approximately. The patient had never undergone a surgical operation before.
His blood tests showed chronic anemia and his tumor markers (CEA, CA 19-9, aFP, and PSA) were within normal limits. The abdominal computed tomography (CT) revealed no other sites of tumor location or other primary sites of squamous malignancy (Fig. 1). Maximum diameter of the tumor was 3 cm in the fundus of the stomach with no suspicious lymph nodes, while the chest CT was normal. The multidisciplinary team decided to proceed to surgery. Three weeks after the multidisciplinary team meeting due to the high volume of the patients, the patient underwent total gastrectomy with Roux-en-Y reconstruction, along with splenectomy and D2 lymphadenectomy. The postoperative recovery was uneventful and the patient was discharged on postoperative day 12.
Pathological assessment of the specimen revealed a 4.7 × 3 × 2.5-cm mass located in the fundus of the stomach invading the subserosa. Out of 48 lymph nodes resected, 9 of them were positive for tumor infiltration. Perineural invasion and extramural venous invasion were also found. The resection margins were free and the final TNM stage was T3N3aM0 (WHO 2017). Microscopically, the tumor was a poorly differentiated gastric squamous cell carcinoma with clear cell characteristics, chronic inflammatory, and desmoplastic stromal reaction (Fig. 2). Immunohistochemistry of gastric tumor confirmed the diagnosis with positive CK14 stain, cyclin-D1 stain, p53 stain, EGFR stain, co-expression of CK5/6, and p63 stains (Figs. 3 and 4). In order to rule out other possible diagnoses or other occult primary tumors, extensive immunohistochemistry check including MUC1, uroplakin III, PAX8, RCC, and PAS was performed without positivity.
Because of the rarity of this specific type of tumor in the stomach, the tumor board decided to rule out other possible primary sites of squamous malignancy. The patient underwent a cranial, abdomen, and chest CT, which revealed enlarged lymph nodes in the mediastinum, in right and left paratracheal area, as well as 4 small bilateral possible secondary lung lesions (Fig. 1). Interestingly enough, these findings were not apparent in the preoperative CT scan. However, they were evident 3 weeks after surgery, while preoperative chest CT scan was unremarkable, a fact that underlines the aggressive behavior of this malignancy. Following that, the patient also underwent bronchoscopy which did not reveal any lesion. Endobronchial brushing results were normal. Full-body FDG PET/CT scan showed multiple metastatic chest lesions of maximum diameter 11 mm (Fig. 1). The patient received adjuvant chemotherapy with paclitaxel and carboplatin. To date, 12 months after the initiation of the chemotherapy, there is no progression of the disease, with minor regression of the metastatic chest lesions.
Primary gastric squamous cell carcinoma (PGSCC) is an extremely rare entity with only a few case reports published so far. Adenocarcinoma accounts for approximately 95% of all gastric malignancies, while PGSCC incidence is only 0.04–0.07%. As far as gender predominance is concerned, male to female ratio is reported to be approximately 4–6/1 [2, 3]. Its prevalence is higher in the sixth decade of life, and the most common tumor location like in our patient seems to be the upper third of the stomach (57.1%), followed by the lower third (21.4%) and the middle third (19.6%) [1, 2]. As in our patient, most of the patients have a long history of smoking, a fact that has been implicated to promote the occurrence of this type of tumor . In this study, 13 patients (61.9%) had a long history of smoking, and according to our observation, like lung squamous carcinoma and esophageal squamous carcinoma, a long history of smoking may promote the occurrence of this tumor.
Diagnostic criteria that were first described in 1967 by Parks were the following: (a) the tumor should not be located at the cardia, (b) the tumor should not extend into the esophagus, and (c) there should be no evidence of SCC in any other parts of the body . All of the above criteria had to be met, but the Japanese Gastric Cancer Association later in 2011 suggested new criteria including the following: (a) all tumor cells have to be SCC cells without any gland cancer cells and (b) SCC must originate in the gastric mucosa . Our patient met the updated criteria for making the diagnosis of PGSCC, as all tumor cells were SCC cells and the lung lesions were metastases from the primary gastric tumor. As there are currently no clinical characteristics that distinguish patients with gastric adenocarcinoma from patients with SCC, histopathological examination is required to confirm the diagnosis . Individual cell keratinization, keratin pearls, intercellular bridges, and positive immunoreactivity for p63 and CK5/6 may be found. Blood examinations, biochemical tests, and tumor serum markers may reveal anemia (66.7%), hypoalbuminemia (42.9%), hypocalcemia (42.9%), elevated values of CEA (38%), and CA19-9 (33.3%) .
Clinical characteristics are not pathognomonic as they are the same with nearly every symptomatic gastric malignant tumor: nonspecific abdominal pain, nausea, vomiting, weight loss, vomiting, melena, bloating, and early satiety . The exact origin and pathogenesis of the tumor is not well known, but several mechanisms have been proposed such as the presence of totipotential (stem) cells, the existence of areas of ectopic squamous cell nests, squamous differentiation of preexisting adenocarcinoma, squamous metaplasia of glandular epithelium secondary to chronic mucosal damage, and SCC arising from the vascular endothelium of the stomach. Furthermore, Epstein-Barr virus infection has been lately implicated in the pathophysiology of the disease [3, 7].
Currently, there is no consensus on how to treat this disease, because of the fact that primary SCC of the stomach is rare and the current evidence is based on case reports and small case series. Radical surgical excision with lymph node dissection remains the main therapeutic approach and has been proposed as the only potential cure for localized disease as it can improve the prognosis of gastric SCC [5, 8, 9]. The efficacy of systemic chemotherapy against the recurrence or metastasis of PGSCC has been demonstrated in some studies [2, 10]. Adjuvant chemotherapy consisting of 5-fluorouracil-based regimens; platin- and taxane-based regimens such as docetaxel + oxaliplatin/cisplatin + fluorouracil, flouorouracil + oxaliplatin + calcium folinate (FOLFOX), capecitabine + oxaliplatin (XELOX); and other combinations has been used effectively in the treatment of PGSCC, offering better outcomes regarding survival, recurrence, and prognosis [5, 6]. Neo-adjuvant chemotherapy for PGSCC seems to be beneficial and efficient but the currently available data remains limited [3, 5, 11].
The prognosis of PGSSC when compared to gastric adenocarcinoma seems to be worse, as it is usually diagnosed at an advanced stage, metastasizing in the liver, lymph nodes, and other organs [3, 12]. Meng et al. reported that median survival of patients with recurrent or metastatic gastric SCC is about 7 months, whereas patients with advanced adenocarcinoma of the stomach show a median survival of 11 months .
Even though clinical features and epidemiological characteristics of PGSCC have been reported in the literature, to date, no standard treatment strategy has been defined. The adoption of current therapeutic strategies of gastric ADC in the management of gastric SCC is debatable, due to differences in molecular characteristics, tissues of origin, and prognosis. The dilemma is whether to manage PGSCC according to therapeutic principles of gastric ADC or that of esophageal SCC. To date, the treatment of PGSCC tends to follow that of gastric ADC; however, a standard chemotherapy regimen for PGSCC has not yet been established. Independently of the optimal chemotherapeutic agent, R0 resection remains the mainstay of the treatment. Multimodality treatments have been applied to improve the overall outcomes of esophageal SCC, especially for patients with locally advanced tumors. Based on several meta-analyses and randomized controlled trials, neoadjuvant chemoradiotherapy, neoadjuvant chemotherapy, and definitive chemoradiotherapy are considered acceptable treatment modalities for locally advanced esophageal SCC in guidelines from the European Society for Medical Oncology (ESMO). However, not much information is available on the role of neoadjuvant chemoradiotherapy in gastric SCC. The optimal multimodality regimen has yet to be defined.
Preoperative radiotherapy (RT) was envisaged to increase the possibility of negative circumferential margins, to lower the loco-regional recurrences and to improve survival. However, there is no randomized control trial (RCT) comparing preoperative RT followed by surgery to surgery alone for PGSCC. Concerning the treatment of esophageal SCC, researchers concluded that there is not enough evidence to suggest that neoadjuvant RT improves the survival of patients with esophageal SCC, implicating that the role of neoadjuvant RT in the management of PGSCC also remains uncertain. To detect reliably a potential benefit of neoadjuvant RT, trials or a meta-analysis would be needed.
Literature search retrieved only a few similar reported cases of PGSCC, with the majority of them describing one single case (Table 1). Numerous previous studies have provided conflicting evidence regarding the optimal therapeutic approach and prognosis of PGSCC. The reported studies indicate that radical surgical excision can improve the prognosis of PGSCC and is the only potential cure for localized disease. Although the effects of chemotherapy on advanced gastric SCC have previously been described in case reports, only a few studies have demonstrated the efficacy of systemic chemotherapy against the recurrence or metastasis of primary SCC of the stomach. In the present study, similar to the cases reported in the literature, we report a case of a 66-year-old male with the preoperative diagnosis of gastric SCC. Radiological imaging and endoscopy were indicative of a T2N0M0 gastric cancer; hence, the multidisciplinary team decided to proceed to surgery, without administration of neoadjuvant treatment. Nonetheless, in our department, we do not routinely perform diagnostic laparoscopy. We performed a total gastrectomy with Roux-en-Y reconstruction, along with splenectomy and D2 lymphadenectomy, followed by adjuvant chemotherapy with paclitaxel and carboplatin.
PGSCC is an extremely rare malignancy of the stomach and seems to be a highly aggressive tumor with poor prognosis. More data and larger series are needed in order to safely decide the best treatment option for these patients and whether adjuvant along with neo-adjuvant treatment plays a significant role in the management of these tumors. Physicians should be aware of its existence, and a high clinical suspicion is required to rule out other possible primary or secondary sites of this specific type of malignancy. An intensive follow-up is imperative after curative surgery, due to the highly aggressive behavior of these tumors.
Availability of data and materials
Primary gastric squamous cell carcinoma
Squamous cell carcinoma
González-Sánchez JA, Vitón R, Collantes E, et al. Primary squamous cell carcinoma of the stomach. Clin Med Insights Oncol. 2017;11:1179554916686076.
Wakabayashi H, Matsutani T, Fujita I, et al. A rare case of primary squamous cell carcinoma of the stomach and a review of the 56 cases reported in Japan. J Gastric Cancer. 2014;14:58–62.
Chen Y, Zhu H, Xu F, et al. Clinicopathological characteristics, treatment, and prognosis of 21 patients with primary gastric squamous cell carcinoma. Gastroenterol Res Pract. 2016;2016:3062547.
Parks RE. Squamous neoplasms of the stomach. Am J Roentgenol Radium Ther Nucl Med. 1967;101:447–9.
Guzman Rojas P, Parikh J, Vishnubhotla P, et al. Primary gastric squamous cell carcinoma. Cureus. 2018;10(3):e2389.
Meng Y, Zhang J, Wang H, et al. Poorer prognosis in patients with advanced gastric squamous cell carcinoma compared with adenocarcinoma of the stomach: case report. Medicine (Baltimore). 2017;96:e9224.
Patnayak R, Reddy V, Radhakrishnan, et al. Primary squamous cell carcinoma of stomach: a rare entity – case report and brief review of literature. J Surg Tech Case Rep. 2015;7:45–7.
Schmidt C, Schmid A, Lüttges JE, et al. Primary squamous cell carcinoma of the stomach. Report of a case and review of literature. Hepatogastroenterology. 2001;48:1033–6.
Callacondo D, Ganoza-Salas A, Anicama-Lima W, et al. Primary squamous cell carcinoma of the stomach with paraneoplastic leukocytosis: a case report and review of literature. Hum Pathol. 2009;40:1494–8.
Marubashi S, Yano H, Monden T, et al. Primary squamous cell carcinoma of the stomach. Gastric Cancer. 1999;2:136–41.
Chang YS, Kim MS, Kim DH, et al. Primary squamous cell carcinoma of the remnant stomach after subtotal gastrectomy. J Gastric Cancer. 2016;16:120–4.
Dursun M, Yaldiz M, Işikdoğan A, et al. Primary squamous cell carcinoma of the stomach: a case report and review of the literature. Eur J Gastroenterol Hepatol. 2003;15:329–30.
Raju GC, Barton EN, Marchack D, Naraynsingh V. Hypercalcaemia in primary squamous cell carcinoma of the stomach. J R Soc Med. 1987 Sep;80(9):587–8.
Hara J, Masuda H, Ishii Y, et al. Exophytic primary squamous cell carcinoma of the stomach. J Gastroenterol. 2004;39(3):299–300.
Choi SB, Park SS, Oh SY, et al. Primary squamous cell carcinoma of the stomach that developed with Menetrier’s disease. Dig Dis Sci. 2007;52(7):1722–4. Epub 2007 Apr 19.
Callacondo D, Ganoza-Salas A, Anicama-Lima W, et al. Primary squamous cell carcinoma of the stomach with paraneoplastic leukocytosis: a case report and review of literature. Hum Pathol. 2009;40(10):1494–8. https://doi.org/10.1016/j.humpath.2009.02.014. Epub 2009 May 20.
Guttmann S, Fromer N, Shamah S, et al. A case of two primary gastric malignancies: adenocarcinoma and squamous cell carcinoma of the stomach. Gastrointest Endosc. 2012;75(5):1113–4. https://doi.org/10.1016/j.gie.2011.05.037. Epub 2011 Jul 29.
Tokuhara K, Nakano T, Inoue K, et al. Primary squamous cell carcinoma in the gastric remnant. Surg Today. 2012;42(7):666–9. https://doi.org/10.1007/s00595-012-0144-6. Epub 2012 Feb 21.
Little M, Munipalle PC, Viswanath YK. Primary squamous cell carcinoma of the stomach: a rare entity. BMJ Case Rep. 2013;2013.
Hwang SH, Lee JH, Kim K, Shin DH, Kim JY, Sol MY, Choi KU. Primary squamous cell carcinoma of the stomach: a case report. Oncol Lett. 2014;8(5):2122–4.
Shi L, Liu FJ, Jia QH, Guan H, Lu ZJ. Synchronous squamous cell carcinoma in the esophagus and stomach: a case report. Turk J Gastroenterol. 2014;25(Suppl 1):244–5.
Mardi K, Mahajan V, Sharma S, Singh S. Primary squamous cell carcinoma of stomach: a rare case report. South Asian J Cancer. 2013;2(4):199.
Gao S, Chen D, Huang L, Dai R, Shan Y. Primary squamous cell carcinoma of the stomach: a case report and literature review. Int J Clin Exp Pathol. 2015;8(8):9667–71.
Modi Y, Shaaban H, Parikh N, Guron G, Maroules M. Primary pure squamous cell carcinoma of the stomach treated with neoadjuvant chemotherapy and surgical resection. Indian J Cancer. 2015;52(1):145.
Wu XD, Zhou Y, Fan RG, Zhou B, Shi Q, Jia J. Primary squamous cell carcinoma of the stomach presenting as a huge retroperitoneal tumor: a case report. Rev Esp Enferm Dig. 2016;108(5):283–4.
Segura S, Pender J, Dodge J, Brandwein SL, El-Fanek H. Primary squamous cell carcinoma of the stomach: a case report and review of the literature. Conn Med. 2016;80(4):209–12.
Gülçiçek OB, Solmaz A, Özdoğan K, Erçetin C, Yavuz E, Yiğitbaş H, Çelebi F, Altınay S. Primary squamous cell carcinoma of the stomach. Ulus Cerrahi Derg. 2015;32(3):221–3.
There was no funding body.
Ethics approval and consent to participate
Consent for publication
Informed consent was obtained from the patient.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Vailas, M.G., Syllaios, A., Hasemaki, N. et al. A type of neoplasia deadlier than gastric adenocarcinoma? Report of a case of primary gastric squamous cell carcinoma. World J Surg Onc 17, 113 (2019). https://doi.org/10.1186/s12957-019-1657-x