A Patient with Duodenal Mucinous Adenocarcinoma Presenting as a Laterally Spreading Tumor

Article information

Clin Endosc. 2015;48(4):336-339
Publication date (electronic) : 2015 July 24
doi : https://doi.org/10.5946/ce.2015.48.4.336
Department of Gastroenterology, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, Seoul, Korea.
Correspondence: Il Hyun Baek. Department of Gastroenterology, Kyung Hee University Hospital at Gangdong, Kyung Hee University School of Medicine, 892 Dongnam-ro, Gangdong-gu, Seoul 134-727, Korea. Tel: +82-2-440-6152, Fax: +82-2-440-8150, topcolon@nate.com
Received 2014 August 19; Revised 2014 October 14; Accepted 2014 October 21.

Abstract

Primary duodenal carcinoma is rare. Duodenal mucinous adenocarcinoma (DMA) is even rarer, and its associated manifestations and typical endoscopic or imaging findings are not well characterized. Herein, we report a case of primary DMA in an asymptomatic 58-year-old man who visited our hospital for a regular health screening. Upper endoscopy revealed an approximately 4-cm lesion in the second portion of the duodenum, but the mass was not visualized on computed tomography. Biopsies revealed a tubular adenoma that was subsequently resected. Frozen biopsies demonstrated DMA with a background of low-grade tubular adenoma for which we performed Roux-en-Y duodenojejunostomy and jejunojejunostomy. To our knowledge, this is the first report of a patient with DMA in Korea.

INTRODUCTION

Primary duodenal mucinous adenocarcinoma (DMA) is very rare. Although the small intestine comprises about 75% of the length and >90% of the surface area of the gastrointestinal (GI) tract, small bowel malignancies account for only 3% of all GI tract neoplasms and approximately 0.5% of all cancers in the United States.1 Adenocarcinomas represent 25% to 40% of small bowel cancers, and the incidence of adenocarcinoma is the highest in the duodenum.2 Mucinous adenocarcinoma, a type of cancer that arises from epithelial cells and produces copious amounts of mucin, has been described in many internal organs including the lungs, ovary, pancreas, appendix, stomach, colon, and rectum, but few cases of DMA have been reported.34

Herein, we describe a patient who underwent Roux-en-Y duodenojejunostomy and jejunojejunostomy for the treatment of DMA.

CASE REPORT

A 58-year-old man with no significant history of medical illness visited our hospital for a regular health screening. He underwent upper endoscopy, during which an approximately 4-cm pinkish mass filling >70% of the lumen of the second portion of the duodenum was noted. The mass was edematous and extended laterally along the side opposite the ampulla. The surface of the mass was irregular and nodular. The tumor was soft and it bled easily at the touch. No mucin or exudates were seen on the lesion (Fig. 1A). Multiple biopsies revealed a tubular adenoma. The patient was admitted to our hospital for further evaluation and surgery.

Fig. 1

Esophagogastroduodenoscopy. (A) A laterally spreading polyp with an irregular surface is visible in the second portion of the duodenum. (B) Follow-up endoscopy after 3 months, showing no evidence of recurrence or abnormal findings at the anastomosis within the duodenum.

On admission, the patient's resting blood pressure was 130/80 mm Hg. He had no significant family medical history, and no symptoms such as abdominal pain, weight loss, or dyspepsia. The results of physical examination were unremarkable. Laboratory data were as follows: white blood cell count, 6,300/mm3 with 64.7% neutrophils; hemoglobin level, 15.6 g/dL; mean corpuscular volume, 96.6 fL; mean corpuscular hemoglobin concentration, 33.5 g/dL; and platelet count, 246,000/mm3. Electrolyte levels and renal and liver functions were all normal. Tests for tumor markers such as carcinoembryonic antigen and carbohydrate antigen revealed no abnormalities, and fecal occult blood test results were negative. Abdominal computed tomography failed to reveal the duodenal mass, and no enlargement of lymph nodes was seen. Findings associated with the liver, pancreas, gallbladder, spleen, kidneys, colon, and rectum were unremarkable, and chest radiography findings were normal.

Two days after his admission, the patient's adenoma was resected. A frozen biopsy showed a 0.7-cm DMA and a background composed of low-grade tubular adenoma with multiple small high-grade foci and in situ carcinoma lesions (Fig. 2). The tumor had invaded the submucosa but not the lymphovascular system, and the resection margins were negative. We then performed Roux-en-Y duodenojejunostomy and jejunojejunostomy. Three months after the surgery, upper endoscopy findings were unremarkable at the duodenal anastomosis site (Fig. 1B). The patient was doing well without any evidence of recurrence at his 1-year follow-up visit.

Fig. 2

Duodenal biopsy histology. These show malignant cells floating in large pools of mucin (A, H&E stain, ×40; B, H&E stain, ×100).

DISCUSSION

Primary small bowel adenocarcinoma (SBA) is a rare malignancy. Compared to colorectal cancer, little is known about the pathogenesis of SBA. SBA is associated with familial adenomatous polyposis, Lynch syndrome, Peutz-Jeghers syndrome, celiac sprue, and Crohn disease.5 The median age at diagnosis of SBA is during the sixth decade of life.6 In the USA, there are approximately 5,300 new cases and 1,100 deaths from SBA per year.7 In Europe, there are approximately 3,600 new cases of SBA every year, and the incidence rate is 5.7 cases per million.8 The incidence of SBA is increasing, mainly because of an associated increase in duodenal tumors.9

It can be difficult to detect SBA owing to its rarity and nonspecific symptoms. However, 43% to 66% of patients with SBA have abdominal pain at the time of diagnosis, and they are often diagnosed during emergencies involving occlusion or bleeding. The diagnosis of SBA is usually made at an advanced stage, and 35% of patients already have metastasis when diagnosed.1011 Therefore, early diagnosis and resection are important for improved outcomes. Negative prognostic factors for SBA include poor tumor differentiation, positive surgical margins, lymph node metastases, extramural venous spread, tumor invasion depth, and Crohn disease.12

Mucinous adenocarcinoma is identified when mucus is present within >50% of an adenocarcinoma, according to the World Health Organization.13 Mucinous adenocarcinoma may arise at various sites, and the prognostic significance of this subtype remains uncertain.

Yasuda et al.14 published a clinicopathological study of mucinous gastric carcinoma (MGC) in which most cases were detected during the advanced stage, and the biological behavior of advanced MGC did not differ from that of other gastric cancers. In their analysis, the majority of MGC cases were ≥5 cm (100%), positive for lymph node metastasis (88%), and positive for serosal invasion (76%). Additionally, their study showed that the mucinous histological type was not an independent prognostic indicator, whereas the prognoses of mucinous carcinoma of the colon and rectum were unfavorable compared with other histological types.15 The prognosis, clinical features, and typical endoscopic findings of DMA remain unclear owing to the rarity of this disease.

Regarding early MGC, restriction to the mucosa is very rare. Hirota et al.16 reviewed the clinicopathological features of 6,288 cases of gastric carcinoma. Among these, MGC comprised 228 cases and early MGC comprised 15 cases, but the frequency of early mucosal MGC was only 0.4% (1/228). These findings may be related to the manner in which MGC develops, as it is thought to arise as a typical gastric carcinoma at an early stage and produce mucin later.17 The typical endoscopic findings of early MGC include an elevated lesion resembling a submucosal tumor due to abundant mucin pools in the submucosa.18 In comparison to early MGC, the DMA described in the current case presented as a laterally spreading tumor at the anti-mesenteric border of the second portion of the duodenum on upper gastroendoscopy. The tumor showed no extracellular mucin or exudate. As the macroscopic appearance of the mass was not consistent with the typical endoscopic findings of mucinous adenocarcinoma, we did not predict that the lesion was a DMA, and the diagnosis was made only after the analysis of a frozen biopsy sample.

With regard to the management of sporadic duodenal adenoma, endoscopy is useful for evaluation and resection. However, in the present case, the mass involved 70% of the lumen and was too large to remove endoscopically. Because resection should be considered for lesions with >33% circumferential involvement of the lumen,19 we chose this treatment method despite the fact that the initial biopsy result had indicated an adenoma.

Our patient had no symptoms or any relevant medical history. Most cases of SBA arise from adenomas; our patient had a DMA with a background of low-grade tubular adenoma. We detected our patient's cancer during a normal health screening and were therefore able to treat it at an early stage, unlike most cases of SBA. In conclusion, primary DMA is a particularly rare tumor and its epidemiology is not yet well defined. Herein, we have reported the first case of DMA in Korea.

Notes

Conflicts of Interest: The authors have no financial conflicts of interest.

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Fig. 1

Esophagogastroduodenoscopy. (A) A laterally spreading polyp with an irregular surface is visible in the second portion of the duodenum. (B) Follow-up endoscopy after 3 months, showing no evidence of recurrence or abnormal findings at the anastomosis within the duodenum.

Fig. 2

Duodenal biopsy histology. These show malignant cells floating in large pools of mucin (A, H&E stain, ×40; B, H&E stain, ×100).