Skip to main content
Diagnostic Pathology logoLink to Diagnostic Pathology
. 2015 Apr 30;10:46. doi: 10.1186/s13000-015-0281-5

Exuberant squamous metaplasia of the gastric mucosa in a patient with gastric adenocarcinoma

Sangjeong Ahn 1, Go Eun Bae 1, Kyoung-Mee Kim 1,
PMCID: PMC4413529  PMID: 25925374

Abstract

Background

The presence of squamous epithelium in the stomach is only occasionally encountered and is associated with prolonged mucosal injury. Squamous metaplasia in patients with cancer is relatively rare and only four cases have been reported in the stomach, all of which have been associated with squamous cell carcinomas. We present the first case of exuberant squamous metaplasia in a patient with gastric adenocarcinoma of the cardia.

Case presentation

A 56-year-old woman presented with epigastric pain and weight loss. Endoscopy showed an irregular depressed hyperemic lesion covered with a whitish plaque on the cardia. A total gastrectomy was performed and the tumor in the subcardia was found to extend up to the proximal stomach with diffuse squamous metaplasia in the surface of the tumor and proximal gastric mucosa in contiguity with the esophageal squamous epithelium. It is believed that the squamous extension from the esophagus to the proximal stomach and the gastric adenocarcinoma occurred at the same time.

Conclusions

Synchronous squamous metaplasia and underlying adenocarcinoma in the stomach is extremely rare. Recognition of this entity would be beneficial for clinicians to avoid unnecessary treatment.

Virtual Slides

The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1035146445160150.

Keywords: Stomach, Squamous metaplasia, Adenocarcinoma

Background

The presence of squamous epithelium in the stomach is only occasionally encountered and is associated with prolonged mucosal injury [1,2]. However, squamous metaplasia with the coexistence of a neoplasm is relatively rare and only 4 cases have been reported in the English literature—4 cases of squamous cell carcinomas (SCC) and 1 case of SCC in situ [3-7]. However, squamous metaplasia associated with gastric adenocarcinoma has not been reported. We present the first case of exuberant squamous metaplasia in a patient with gastric adenocarcinoma of the cardia.

Case presentation

A 56-year-old Korean woman presenting with epigastric pain and weight loss visited a local clinic and was transferred to our hospital for further treatment. The medical history of the patient did not include any significant prior illness. No significant positive signs were found on physical examination. Endoscopy showed an irregular depressed hyperemic lesion covered with a whitish plaque on the cardia (Figure 1). The lesion was approximately 4 cm in diameter and the whitish plaque was partly contiguous with the esophageal mucosa at the gastroesophageal junction. The biopsy specimen revealed infiltrating neoplastic single cells with benign squamous epithelium (Figure 2). Laboratory results were within normal limits, and serum carcinoembryonic antigen (CEA) levels and carbohydrate antigen 19–9 (CA 19–9) levels were normal. A total gastrectomy was performed without any surgical complications.

Figure 1.

Figure 1

Endoscopic findings of the stomach. An area of white mucosa was found in the cardia contiguous to the esophageal mucosa. On the edge of this area, an irregular and slightly depressed hyperemic lesion was observed.

Figure 2.

Figure 2

The biopsy specimen showed infiltrating neoplastic signet ring cells beneath benign squamous epithelium.

On gross examination, an irregular depressed lesion with a whitish plaque was detected in the high body (Figure 3A). Entire tumor was sampled for histologic examinations. Histological examination revealed poorly differentiated tubular adenocarcinoma that was diffuse-type. The tumor was centered in the subcardia extending up to the proximal stomach without involvement of the gastroesophageal junction (type III by the Siewert classification) [8] (Figure 3B). Diffuse squamous metaplasia was present in the surface of the tumor and the proximal gastric mucosa in contiguity with the esophageal squamous epithelium (Figure 4). We performed EBER in situ hybridization and the entire tumor was negative. The tumor infiltrated into the muscularis propria although none of the 54 regional lymph nodes showed metastasis (pT2N0M0, stage IB by the 7th edition of the AJCC/TNM classification). The patient is alive without recurrence 3 month after gastrectomy.

Figure 3.

Figure 3

Gross and schematic photos. (A) Grossly, an irregular depressed lesion with whitish plaque was detected. (B) Histological examination revealed a tumor (red) that was centered in the subcardia extending up to the proximal stomach. Diffuse squamous metaplasia (blue) was present in the surface of the tumor and proximal gastric mucosa in contiguity with the esophagus squamous epithelium (yellow).

Figure 4.

Figure 4

Microscopic findings of total gastrectomy specimen showing esophagus, gastroesophageal junction and squamous metaplasia with underlying gastric adenocarcinoma.

Discussions

Although the pathophysiology of squamous metaplasia in the stomach remains obscure, prolonged injury appears to be a prerequisite for this mucosal abnormality. The presence of squamous epithelium in the gastric mucosa has been described in patients with underlying diseases such as peptic ulcer [9], tuberculosis [10], syphilis [4], corrosive gastritis [3], pernicious anemia [11], and aberrant pancreatic tissue [12]. These cases support the hypothesized relationship between injurious stimuli and the development of squamous metaplasia. In animal studies, gastric squamous metaplasia has been induced by the injection of pyrogallic acid [13] and methylcholanthere [14]. Squamous metaplasia following chronic irritation occurs elsewhere in the body, for example in the lower respiratory tract, bladder, salivary duct, pancreatic duct, cecum, uterus, and in the mucosa of the prolapsed rectum.

The four patients with squamous metaplasia in the stomach and concurrent carcinoma who have been recorded in the literature are tabulated in Table 1 along with pertinent details given by the authors [3-6]. The stomach from all four patients contained areas of squamous metaplasia transitioning to SCC, corroborating the development of SCC from the squamous metaplasia. The patients in cases 1 to 3 had prior a history of prolonged gastritis provoked by sustained mucosal injuries. The gastric mucosa of the patient in case 1 [3] was damaged by acid and the entirety of the stomach was lined by squamous epithelium. The patient in case 2 [4] was diagnosed with congenital syphilis, progressed to chronic syphilitic gastritis, and had squamous metaplasia in the antrum. The stomach of the patient in case 3 showed diffuse gastritis due to prior cytotoxic chemotherapy for malignant lymphoma [5].

Table 1.

Cases of squamous metaplasia with gastric neoplasm reported in the literature

No Age/Sex Symptom Location (T/SM) Size (T/SM) Gross findings (T/SM) Associated neoplasm Clinical information Reference
1 30/M Dysphagia Body/body NA/NA Ulcerative granular area/NA Squamous cell carcinoma History of ingestion of corrosive acid many years earlier [3]
2 49/F Epigastric pain Low body of greater curvature/antrum NA/2.2 cm Polypoid mass/whitish irregular mucosal plaque Squamous cell carcinoma Congenital syphilis with chronic syphilitic gastritis [4]
3 55/M Epigastric pain Upper body of lesser curvature/anterior wall of cardia 8 cm/NA Polypoidgray white, granular tumor/patch of grey-white, shiny mucosa Squamous cell carcinoma Diffuse gastritis due to prior cytotoxic chemotherapy for lymphoma [5]
4 71/M NA Lesser curvature of Cardia/Lesser curvature of cardia 0.8 cm/NA Irregular whitish depressed lesion/NA Squamous cell carcinoma in situ NA [6]
5 69/M Epigastralgia Lesser curvature of cardia/Lesser curvature of cardia 2.1 cm/NA Superficial and protruding tumor/whitish mucosa Squamous cell carcinoma EBV infection [7]
Case 56/F Epigastric pain Cardia/cardia 4.5 cm/2.5 cm Irregular depressed lesion/whitish plaque Adenocarcinoma Intestinal metaplasia

T = tumor; SM = squamous metaplasia; NA = not available.

In contrast to these previously reported cases, our case was unique in that the benign squamous epithelium covering the tumor surface was in continuity with the esophageal epithelium without any transition area. Endoscopic and microscopic findings revealed diffuse mucosal atrophy with intestinal metaplasia, which is considered to be a risk factor for gastric adenocarcinoma [15]. Based on the above observations, we hypothesize that the squamous extension from the esophagus to the proximal stomach and the adenocarcinoma occurred at the same time, which is an exceedingly rare event.

The tumor topography of the border between the esophagus and stomach affects the treatment strategy that for patients with type II tumors by the Siewert classification, with esophagectomy offering no advantages over extended gastrectomy [8]. The biopsy specimen in our case showed infiltrating cancer cells beneath the benign squamous epithelium, which could be misinterpreted as adenocarcinoma at the esophagogastric junction or invasion into the esophagus. The endoscopic findings showed gastric extension of whitish plaque in contiguity with the esophagus. Microscopically, the proximal gastric mucosa showed diffuse squamous metaplasia with no evidence of carcinoma. Therefore, the possibility of squamous metaplasia in the stomach should be considered to avoid unnecessary treatment such as proximal esophagectomy. If the squamous metaplasia is too small to recognize, Lugol’s iodine solution would be helpful for staining the metaplastic area [6].

Conclusions

Synchronous squamous metaplasia and underlying adenocarcinoma in the stomach is extremely rare. Here, we describe the first case with unique endoscopic findings.

Consent

Written informed consent was obtained from the patient for the publication of this report and any accompanying images.

Acknowledgement

This study was supported by a grant from the 20 by 20 project of Samsung Medical Center (GF01140111).

Abbreviations

SCC

Squamous cell carcinomas

CEA

Carcinoembryonic antigen

CA 19–9

Carbohydrate antigen 19–9

AJCC

American Joint Committee on Cancer

T

Tumor

SM

Squamous metaplasia

NA

Not available

Footnotes

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

KEB first identified this case and participated in providing the clinical information, KMK contributed to the concept and design and approved the final version of the manuscript and SA wrote the manuscript and performed the literature review. All authors read and approved the final manuscript.

Contributor Information

Sangjeong Ahn, Email: vanitasahn@gmail.com.

Go Eun Bae, Email: hisilver.bae@samsung.com.

Kyoung-Mee Kim, Email: kkmkys@skku.edu.

References

  • 1.Takeda H, Nagashima R, Goto T, Shibata Y, Shinzawa H, Takahashi T. Endoscopic observation of squamous metaplasia of the stomach: a report of two cases. Endoscopy. 2000;32:651–3. doi: 10.1055/s-2000-9017. [DOI] [PubMed] [Google Scholar]
  • 2.Fass R, Garewal HS, Hayden CW, Ramsey L, Sampliner RE. Preferential repair by squamous epithelium of thermal induced injury to the proximal stomach in patients undergoing ablation of Barrett’s esophagus. Gastrointest Endosc. 2001;53:711–6. doi: 10.1067/mge.2001.114781. [DOI] [PubMed] [Google Scholar]
  • 3.Eaton H, Tennekoon GE. Squamous carcinoma of the stomach following corrosive acid burns. Br J Surg. 1972;59:382–7. doi: 10.1002/bjs.1800590514. [DOI] [PubMed] [Google Scholar]
  • 4.Vaughan WP, Straus FH, 2nd, Paloyan D. Squamous carcinoma of the stomach after luetic linitis plastica. Gastroenterology. 1977;72:945–8. [PubMed] [Google Scholar]
  • 5.Callery CD, Sanders MM, Pratt S, Turnbull AD. Squamous cell carcinoma of the stomach: a study of four patients with comments on histogenesis. J Surg Oncol. 1985;29:166–72. doi: 10.1002/jso.2930290307. [DOI] [PubMed] [Google Scholar]
  • 6.Oono Y, Fu K, Nagahisa E, Kuwata T, Ikematsu H, Yano T, et al. Primary gastric squamous cell carcinoma in situ originating from gastric squamous metaplasia. Endoscopy. 2010;42(Suppl 2):E290–1. doi: 10.1055/s-0030-1255807. [DOI] [PubMed] [Google Scholar]
  • 7.Takita J, Kato H, Miyazaki T, Nakajima M, Fukai Y, Masuda N, et al. Primary squamous cell carcinoma of the stomach: a case report with immunohistochemical and molecular biologic studies. Hepatogastroenterology. 2005;52:969–74. [PubMed] [Google Scholar]
  • 8.Rudiger Siewert J, Feith M, Werner M, Stein HJ. Adenocarcinoma of the esophagogastric junction: results of surgical therapy based on anatomical/topographic classification in 1,002 consecutive patients. Ann Surg. 2000;232:353–61. doi: 10.1097/00000658-200009000-00007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Boswell JT, Helwig EB. Squamous cell carcinoma and adenoacanthoma of the stomach. A clinicopathologic study. Cancer. 1965;18:181–92. doi: 10.1002/1097-0142(196502)18:2<181::AID-CNCR2820180209>3.0.CO;2-3. [DOI] [PubMed] [Google Scholar]
  • 10.Watson GW, Flint ER, Stewart MJ. Hyperplastic tuberculosis of the stomach causing hour-glass deformity, with complete squamous metaplasia of the upper loculus. Br J Surg. 1936;24:333–40. doi: 10.1002/bjs.1800249413. [DOI] [Google Scholar]
  • 11.Tolia V, Chang CH, Emami A. Juvenile onset pernicious anemia, partial intestinal villous atrophy, ulcerative colitis, and squamous metaplasia of the stomach. Am J Gastroenterol. 1986;81:803–7. [PubMed] [Google Scholar]
  • 12.Yamagiwa H, Yosimura H, Nishii M, Moriyama S. [Squamous metaplasia of the gastric mucosa associated with an aberrant pancreas] Gan No Rinsho. 1987;33:1929–32. [PubMed] [Google Scholar]
  • 13.FüTterer G. Experimentally produced genuine epithelial metaplasia in the stomachand the relations of epithelial metaplasia to carcinoma, as demonstrated by cases reported in the literature. JAMA. 1904;43:1129–40. doi: 10.1001/jama.1904.92500160001h. [DOI] [Google Scholar]
  • 14.Hare WV, Stewart HL, Bennett JG, Lorenz E. Tumors of the glandular stomach induced in rats by intramural injection of 20-methylcholanthrene. J Natl Cancer Inst. 1952;12:1019–55. [PubMed] [Google Scholar]
  • 15.Uemura N, Okamoto S, Yamamoto S, Matsumura N, Yamaguchi S, Yamakido M, et al. Helicobacter pylori infection and the development of gastric cancer. N Engl J Med. 2001;345:784–9. doi: 10.1056/NEJMoa001999. [DOI] [PubMed] [Google Scholar]

Articles from Diagnostic Pathology are provided here courtesy of BMC

RESOURCES