World J Gastroenterol. 2006 September 14; 12(34): 5573-5576.
Published online 2006 September 14. doi: 10.3748/wjg.v12.i34.5573.
©2006 Baishideng Publishing Group Co., Limited. All rights reserved.
Mucosa-associated lymphoid tissue lymphoma of the transverse colon: A case report
Shigetoshi Matsuo, Seiya Susumu, Ryuji Tsutsumi, Takashi Azuma, Satoshi Yamaguchi, Department of Surgery, Nagasaki Prefectural Shimabara Hospital, Shimabara, Nagasaki, Japan
Yohei Mizuta, Second department of Internal medicine, Nagasaki University School of Medicine, Nagasaki, Japan
Tomayoshi Hayashi, Department of Pathology, Nagasaki Prefectural Shimabara Hospital, Shimabara, Nagasaki, Japan
Received June 7, 2006; Revised June 28, 2006; Accepted July 7, 2006;
We herein present a case of a 75-year-old female with mucosa-associated lymphoid tissue (MALT) lymphoma of the transverse colon with the stage IE (Ann Arbor classification). Colonoscopy revealed the tumor’s appearance as a IIa plus IIc-like early colon cancer as defined according to the macroscopic classification of the Japanese Research Society for Cancer of Colon, Rectum and Anus, measuring less than 2 cm in diameter. Histologically, the tumor was diagnosed as MALT lymphoma because of the presence of lymphoepithelial lesions consisting of diffuse proliferation of atypical lymphocytes and glandular destruction. The majority of these lymphocytes immunohistochemically stained for the B-lymphocyte marker. The patient first underwent H pylori eradication therapy with Lansap®. However, the tumor size gradually increased over the next 4 mo and the patient eventually underwent surgical resection. The operative procedure included a partial colectomy with dissection of the paracolic lymph nodes. The tumor measured 45 mm x 30 mm in diameter and histological examination showed that the lymphoma cells had infiltrated the muscle layer of the colon without nodal involvement. The patient has had no recurrence postoperatively without any chemotherapy.
Keywords: Mucosa-associated lymphoid tissue, Malignant lymphoma
The term mucosa-associated lymphoid tissue (MALT) lymphoma was first introduced by Isaacson and Wright[1
] in 1983. This entity includes low-grade gastric B-cell lymphoma and immunoproliferative small intestinal disease. MALT lymphomas occur in a variety of extra-nodal organs, such as the gastrointestinal (GI) tract and the non-GI tract, in which the stomach is the most common site[2,3
]. Since convincing evidence has been presented showing the relationship between H pylori
and gastric MALT lymphoma, the therapeutic strategy has been altered for patients with gastric MALT lymphoma in the early stages[4-8
]. In contrast, a treatment for colonic MALT lymphoma has not yet been established. In the present report, we describe a case of colonic MALT lymphoma which did not response to H pylori
eradication treatment and, therefore, underwent a surgical resection, and also provide a literature review on this rare entity.
A 75-year-old female was admitted to Nagasaki Prefectural Shimabara Hospital for surgical treatment of MALT lymphoma of the transverse colon on June 21, 2005. The patient had shown a positive fecal occult blood test on January 20, 2005 without any clinical symptoms and signs. Her past histories included hypertension, diabetes mellitus, and cholecystolithiasis. The results of complete blood counts, blood chemistries and tumor markers, such as carcinoembryonic antigen, were all within the normal limits. Colonoscopy revealed the tumor’s appearance as IIa plus IIc-like early colon cancer[9
], measuring less than 2 cm in diameter, in the transverse colon (Figure ). Biopsy specimens histologically showed lymphoepithelial lesions with diffuse proliferation of atypical small lymphocytes and some glandular destruction. These lymphocytes immunohistochemically showed diffusely positive staining for L-26 (Figure ) and bcl-2, but negative staining for CD3, CD5, CD10, CD79a, UCHL-1 and cyclin D1. These findings were compatible with MALT lymphoma of the colon. Barium enema showed a flat-elevated lesion in the transverse colon (Figure ). Abdominal and chest CT demonstrated neither abnormal lesions nor enlargement of lymph node. According to the Ann Arbor classification, this MALT lymphoma belonged to the stage IE. The patient first underwent H pylori
eradication therapy with Lansap®
because of positive reaction to a urea breath test (UBT). However, over the course of 4 mo, the tumor gradually increased in size, although H pylori
were eradicated. The patient was considered to be a non-responder to eradication therapy, and was indicated for surgical resection. A partial colectomy with dissection of the paracolic lymph nodes was performed on June 23, 2005 (Figure ). The tumor grossly appeared to be a IIa plus IIc-like early colon cancer, measuring 45 mm × 30 mm in diameter. Resected specimens were histologically and immunohistochemically reconfirmed to be MALT lymphoma without nodal involvement. The lymphoma cells infiltrated mainly into the mucosa and submucosal layer, and partly infiltrated into the muscular layer of the colon (Figure ). The patient has had no recurrence postoperatively without any chemotherapy.
Colonofiberscopy showing the tumor’s appearance as a IIa plus IIc-like early colon cancer.
Biopsy specimens histologically showing diffuse proliferation of atypical small lymphocytes in the mucosal layer (A: x 40 magnification, HE) and glandular destruction (B: x 200 magnification, HE). These lymphocytes immunohistochemically showing diffusely positive staining for L-26 (C; x 200 magnification, ABC method).
Barium enema showing a flat and well-circumscribed tumor in the transverse colon (arrows).
Resected specimens showing a flat-elevated tumor with slight depression, measuring 45 mm x 30 mm in diameter.
The lymphoma cells mainly infiltrated into the mucosal and submucosal layers, and partly infiltrated into the muscular layer of the colon (x 20 magnification, HE).
MALT lymphoma is defined as extra-nodal marginal zone B-cell lymphoma of MALT type in peripheral B-cell lymphoma according to morphologic features, immunophenotype, genetic features, postulated normal counterpart, and clinical features[10,11
eradication therapy is currently widely recognized as an initial therapy in cases with low-grade (stage I) gastric MALT lymphoma[12-14
]. In contrast, it has not yet been clarified whether H pylori
eradication, or chemotherapy, or surgery should be performed in colonic MALT lymphoma compared with gastric MALT lymphoma, because the colorectal MALT lymphomas are rare. The individual clinical details of colorectal MALT lymphoma are summarized in Table [15-27
]. Some reports have described the successful regression of colorectal MALT lymphoma by means of eradication therapy in H pylori
]. Even in cases with colorectal MALT lymphoma negative for H pylori
, the regression of the tumor was also recognized as a result of H pylori
]. In prospective studies of gastric MALT lymphoma, eradication therapy was not effective in patients negative for H pylori
]. Grunberger et al[30
] reported that antibiotic eradication therapy was not effective in patients infected with H pylori
suffering from extra-gastric MALT lymphoma. Therefore, they suggested that H pylori
did not play a role in the development of extra-gastric MALT lymphomas. Similarly, antibiotic eradication therapy was not effective in our present case. These results may suggest that colorectal MALT lymphomas are not directly related to H pylori
infection, while gastric MALT lymphomas are strongly associated with H pylori
infection. In the future, a definite pathogenesis of colorectal MALT lymphoma should be clarified when cases of colorectal MALT lymphomas have accumulated. As a speculation, colorectal MALT lymphomas may be caused by unknown antibiotic-sensitive microorganisms other than H pylori
, although that is not clear. In gastric MALT lymphoma, indeed, Helicobacter heilmannii
-associated MALT lymphoma other than H pylori
has been reported to be completely regressed by eradication therapy[31
Colorectal MALT lymphoma in the English literatures
Surgical resection is mandatory when a colorectal MALT lymphoma does not respond to eradication therapy or chemotherapy, and it is localized without dissemination.
In conclusion, the present case with colonic MALT lymphoma eventually underwent surgical resection of the colon after the failure of eradication therapy. Surgical intervention is now the procedure of choice for colorectal MALT lymphoma because its pathogenesis and therapeutic strategy have not yet been established.
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