- Case Report
- Open Access
Rectal hodgkin lymphoma in a patient with ulcerative colitis: a case study
Diagnostic Pathologyvolume 10, Article number: 25 (2015)
A case of Hodgkin lymphoma located in the rectum of a patient with ulcerative colitis is described. The patient was a 44 year old male treated with thiopurines for ulcerative colitis for ten years. He was admitted with malaise, weight loss and abdominal pain. Endoscopy revealed a large ulcerative lesion involving the rectum and distal part of the sigmoid colon. Although it macroscopically resembled a rectal cancer, repeated biopsies did not reveal any malignancy. In order to resolve the symptoms of stenosis and to get the final diagnosis a recto-sigmoid resection was performed. Pathologic examination revealed nodular sclerosis classical Hodgkin lymphoma, positive for Epstein Barr Virus. Subsequent examination revealed disseminated disease involving the pelvic wall, liver, and bone marrow. The patient is currently receiving chemotherapeutic treatment, and follow-up shows disease remission.
Hodgkin lymphoma associated with immunosuppressive therapy is rare. However, patients with ulcerative colitis receiving such treatment are at increased risk of lymphoproliferative disordes, potentially due to loss of immunosurveillance and presence of oncogenic viruses (i.e. Epstein-Barr virus).
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Hodgkin lymphoma (HL) is a relatively rare disease with an estimated 9.190 new cases in the United States in 2014 .Primary extranodal lymphomas of the gastrointestinal tract are rare. Lymphomas only account for 0.2-0.6% of large bowel malignancies  and primary HL involving the gastrointestinal tract is only reported in a limited number of case reports [3-5].
Most patients with HL do not have a history of immunodeficiency, but a small subset of cases arise in patients with acquired immunodeficiency (e.g. patients suffering from human immunodeficiency virus) and patients receiving immunomodulatory therapeutic agents (e.g. patients who have received organ transplants) [6,7].
In this report, a rare case of an advanced stage HL diagnosed in the rectum and sigmoid colon of patient with ulcerative colitis is presented.
A 44 year old male presented in 2004 with a history of abdominal pain, intermittent diarrhoea, and rectal bleeding. A colonoscopy was performed, and severe inflammation was found in the recto-sigmoid mucosa. The clinical, endoscopic, and pathologic findings were consistent with ulcerative colitis. Initial medical treatment was Azathioprine (50 mg, three times a day), Prednisolone (50 mg, one time a day), and 5-aminosalicylic acid (800 mg, three times a day). The patient was continually treated with Azathioprine through ten years. On multiple occasions, he was admitted with exacerbations, and treated with Prednisolone and 5-aminosalicylic acid.
In 2014, the patient experienced malaise, weight loss, night sweat, and intermittent fever for three to four months before admission. Sigmoideoscopy showed a large ulcerative lesion obstructing the recto-sigmoid colon (Figure 1). Multiple biopsies did not reveal malignancy but macroscopically it was believed to be a colorectal cancer. In order to resolve the symptoms of stenosis and to reveal the final diagnosis, a partial recto-sigmoid resection was performed. The workup of the patient was initially delayed by a simultaneous bilateral pulmonary embolism, for which the patient needed treatment with low molecular weight heparin.
The recto-sigmoid resection specimen showed a deep ulcer measuring 4 × 5 cm with relatively sharp edges (Figure 2A). Corresponding to the ulcer there was a tumorous swelling of the serosa, which was dark and granulated.
Histological evaluation of the ulcer revealed nodular sclerosis classical HL, with Hodgkin and Reed-Sternberg cells surrounded by nodular infiltrates of lymphocytes, plasma cells and eosinofilic granulocytes, in the muscularis propria and subserosa (Figure 2C). Immunohistochemically, the Hodgkin and Reed-Sternberg cells stained positive for CD15, CD30, PAX5 (weak), and fluorescence in situ hybridization for EBER (Epstein–Barr virus-encoded small RNAs) was positive (Figure 2D-F).
At the same time focal extranodal, but no nodal, involvement of the sigmoid and rectal serosa, the sigmoid mesocolon and the peritoneum of the urinary bladder was demonstrated histologically.
Postoperative course and treatment
Postoperative positron emission tomography-computed tomography (PET-CT), revealed advanced stage disease, with increased metabolic activity in the liver, pelvic muscles, and bone marrow in the thoracic region (Figure 3).
Four months after the surgery, the patient had received six of twelve rounds of chemotherapeutic treatment, with Adriamycin, Bleomycin, Vinblastine, and Dacarbazine. Follow-up PET-CT has shown near complete metabolic remission.
Patients with ulcerative colitis are at increased cancer risk, especially with regard to colorectal adenocarcinoma, with annual incidence rates being elevated by close to 30%, compared to patients without inflammatory bowel disease (IBD) . However, a recent study was not able to reproduce this increased risk when stratifying for treatment with immunomodulating agents (including thiopurines) .Whether the risk of malignant lymphoma in patients with IBD is increased is controversial. Recent studies have found no, or only a marginally elevated risk of lymphoproliferative disorders [9-11]. However, it has been shown that the risk of developing lymphoproliferative disorders is increased in IBD as well as other patients receiving thiopurines as treatment (HR, 5.28; 95% CI, 2.01-13.9) . An increased incidence of lymphomas in IBD patients could, therefore, be attributed to treatment with immunosuppressive drugs. A study on patients with rheumatoid arthritis showed that high inflammatory activity was a risk factor for lymphoma development (OR, 5.8; 95% CI, 3.1-213) , and it has been speculated that the same could be the case in patients with ulcerative colitis .
HL attributed to treatment with immunosuppressive drugs is very rare and only described in case studies. These cases are primarily described in patients with rheumatoid arthritis and Crohn’s disease, promoting IBD patients treated with immunosuppressants as a group a higher risk . The majority of cases described were also positive for Epstein-Barr virus promoting oncogenic viral infection as an additional risk factor .
The diagnosis of extranodal HL can be a challenge. Classical HL is based on the identification of mononucleated Hodgkin cells and multinucleated giant cells termed Reed-Sternberg cells, within an inflammatory environment . The Hodgkin and Reed-Sternberg cells are however, vastly outnumbered by reactive inflammatory cells, which constitute from 90–99.9% of the tumour mass .
In the present case, the initial biopsies only showed chronic ulcer, while surgical resection provided material from the deeper parts of the gut wall, which revealed the final diagnosis. The preoperative biopsies were reviewed with the disease in mind, but no Reed-Sternberg cells could be distinguished.
The patient had received treatment with both thiopurines (continually) and 5-aminosalicylic acid (intermittently) through ten years. Special attention should be given to such patients, when they present symptoms that are not characteristic of their known inflammatory disease, as their risk of lymphoproliferative disorders is increased. Even though extranodal presentation of HL is a rare entity, the possibility should be kept in mind, as survival relies on early and efficient treatment.
Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Postoperative positron emission tomography-computed tomography
Inflammatory bowel disease
Siegel R, Ma J, Zou Z, Jemal A. Cancer Stat. 2014;2014:9–29.
Wong MTC, Eu KW. Primary Colorectal Lymphomas. 2006. p. 586–91.
Hall AG, Taylor R, Evans RG, Curtis M, Proctor SJ. Hodgkin’s Disease Involving the Large Bowel. 1988. p. 193–4.
Zemsky L, Katz H, Edelman M, Makower D. Hodgkin’s Disease Involving the Large Bowel. 2001. p. 185–6.
Thomas DB, Huston BM, Lamm KR, Maia DM. Primary Hodgkin’s Disease of the Sigmoid Colon: A Case Report and Review of the Literature. 1997. p. 528–32.
Garnier JL, Lebranchu Y, Dantal J, Bedrossian J, Cahen R, Assouline D, et al. Hodgkin’s Disease after Transplantation. 1996. p. 71–6.
Glaser SL, Clarke CA, Gulley ML, Craig FE, DiGiuseppe JA, Dorfman RF, et al. Population-Based Patterns of Human Immunodeficiency Virus-Related Hodgkin Lymphoma in the Greater San Francisco Bay Area, 1988–1998. 2003. p. 300–9.
Herrinton LJ, Liu L, Levin TR, Allison JE, Lewis JD, Velayos F. Incidence and mortality of colorectal adenocarcinoma in persons with inflammatory bowel disease from 1998 to 2010. 2012;382–9.
Jess T, Horváth-Puhó E, Fallingborg J, Rasmussen HH, Jacobsen BA. Cancer Risk in Inflammatory Bowel Disease According to Patient Phenotype and Treatment: A Danish Population-Based Cohort Study. 2013. p. 1869–76.
Lewis JD, Bilker WB, Brensinger C, Deren JJ, Vaughn DJ, Strom BL. Inflammatory Bowel Disease is not Associated with an Increased Risk of Lymphoma. 2001. p. 1080–7.
Askling J, Brandt L, Lapidus A, Karlén P, Björkholm M, Löfberg R, et al. Risk of Haematopoietic Cancer in Patients With Inflammatory Bowel Disease. 2005. p. 617–22.
Beaugerie L, Brousse N, Bouvier AM, Colombel JF, Lémann M, Cosnes J, et al. Lymphoproliferative Disorders in Patients Receiving Thiopurines for Inflammatory Bowel Disease: A Prospective Observational Cohort Study. 2009. p. 1617–25.
Baecklund E, Ekbom A, Sparén P, Feltelius N, Klareskog L. Disease Activity and Risk of Lymphoma in Patients with Rheumatoid Arthritis: Nested Case–Control Study. 1998. p. 180–1.
Jones JL, Loftus EV. Lymphoma Risk in Inflammatory Bowel Disease: is it The Disease or its Treatment? 2007. p. 1299–307.
Loo EY, Medeiros LJ, Aladily TN, Hoehn D, Kanagal-Shamanna R, Young KH, et al. Classical Hodgkin Lymphoma Arising in The Setting of Iatrogenic Immunodeficiency: A Clinicopathologic Study of 10 Cases. 2013. p. 1290–7.
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, Fourth Edition. 2008. p. 439.
This manuscript was developed through collaboration between the Department of Gastrointestinal Surgery and the Institute of Pathology, Aalborg University Hospital.
The authors wish to thank, Professor Ole Thorlacius-Ussing and Professor Mogens Vyberg for their contribution, supervision, and review of the article.
The authors wish to thank, Ilse Christiansen, from the Department of Hematology, Aalborg University Hospital, for her reflections on the article.
The authors wish to thank, Magdalena Kubik, from the Department of Nuclear Medicine, Aalborg University Hospital, for her contribution and interpretation of the PET-CT images used in the article.
The authors declare that they have no competing interests.
SLR included the patient, made the clinical case description and drafted the manuscript. CT analyzed the histological sections and helped draft the manuscript. All authors read and approved the final manuscript.