| Home | E-Submission | Sitemap | Contact Us
Korean J Intern Med > Volume 29(1); 2014 > Article
Kook, Yhim, Lee, Song, Kim, Yim, and Kwak: Successful treatment of myelodysplastic syndrome and Behcet colitis after allogeneic hematopoietic stem cell transplantation
To the Editor,
Myelodysplastic syndrome (MDS) is a heterogeneous group of stem cell disorders of unknown etiology. Behcet disease (BD) is a systemic autoimmune vasculitis also of unknown cause. Several recent reports have suggested an association between MDS and BD [1], possibly related to a cytogenetic abnormality such as trisomy 8 [2]. In addition, some distinctive clinical characteristics have been identif ied that include a high frequency of intestinal BD, generally high disease activity, and a trend toward treatment with more potent immunosuppressive therapy [2,3]. The treatment of MDS-related Behcet colitis is usually diff icult to manage, and many patients eventually die of infection or hemorrhage. We herein report a case of intractable MDS-related Behcet colitis that was successfully treated by allogeneic hematopoietic stem cell transplantation (HSCT).
A 38-year-old female was admitted to our hospital with complaints of recurrent abdominal pain and fever. In June 2001, she was diagnosed with BD according to the diagnostic criteria of the international BD study group [4]. She had bouts of several symptoms compatible with BD, such as recurrent nasal ulcers, oral ulcers, genital ulcers, migrating arthralgia, and uveitis. Total colonoscopy performed to evaluate the recurrent abdominal pain revealed a shallow ulceration of 2 × 2 cm with irregular margins in the ileocecal area (Fig. 1A). Pathologic examination showed chronic ulcerative inflammation with lymphocyte infiltration compatible with Behcet colitis (Fig. 2). She was followed closely at the rheumatology clinic and initially treated with corticosteroids alone; however, this treatment produced no relief of symptoms. Azathioprine was added, but she continued to experience recurrent abdominal pain. Sulfasalazine was administered without improvement. In spite of active management of Behcet colitis, the abdominal pain persisted in a waxing and waning manner. In April 2005, her complete blood count (CBC) values gradually decreased, particularly the leukocyte count (2.86 × 103/µL) and hemoglobin level (8.3 g/dL). In May 2008, the CBC showed further decreases in the leukocyte count (1.70 × 103/µL) and hemoglobin level (5.1 g/dL), and thrombocytopenia (90.0 × 103/µL) was detected. Bone marrow examination revealed trilineage dysplasia with less than 5% blasts. Chromosomal analysis of bone marrow aspirates showed trisomy 8. She was diagnosed with MDS with refractory cytopenia with multilineage dysplasia. According to the International Prognostic Scoring System, the disease was classified as intermediate-1. For further evaluation and therapeutic options, she was referred to our hematology clinic. She started treatment with decitabine because she did not have a human leukocyte antigen (HLA)-matched sibling donor. However, recurrent infections developed with complications such as neutropenic fever, pneumonia, and hepatosplenic candidiasis. Decitabine was stopped and hematologic supportive care begun with intermittent red cell transfusion at intervals of ~2 weeks for 15 months. We had intermittently been searching for unrelated donors from the public blood and marrow donation program since the diagnosis of MDS. Finally, a fully matched HLA-compatible unrelated donor was found in January 2010. Until that time, recurrent oral ulcers, migrating arthralgia, and abdominal pain had persisted, and she often required several days of hospitalization to modulate the pain and associated symptoms such as diarrhea. The patient underwent allogeneic peripheral blood stem cell transplantation with a myeloablative regimen in April 2010. The pretransplantation conditioning regimen comprised busulfan and cyclophosphamide. An infusion of 4.6 × 106/kg CD34+ cells was introduced. Methotrexate and cyclosporine were used routinely for graft-versus-host disease (GVHD) prophylaxis. On day 12, leukocyte engraftment was observed. Cyclosporine was discontinued on day 189, and abdominal pain was markedly diminished. On day 229 after transplantation, total colonoscopy was repeated. The previous lesion was greatly improved, and only a small shallow ulceration was observed (Fig. 1B). There was no need to treat for Behcet colitis. At the time of this report, the patient was doing well in complete remission of MDS without evidence of chronic GVHD and no signs or symptoms of BD.
MDS is an acquired clonal disorder of hematopoietic progenitor cells. Several recent studies showed that an autoimmune mechanism plays an important role in the development of MDS, and another study suggested that transformation of normal stem cells induces an autoimmune T cell response. Although MDS and BD have been regarded as different manifestations, the same pathophysiological processes, such as abnormal neutrophil function, overproduction of inf lammatory cytokines, and immunological abnormalities, are thought to be related to MDS and BD [1]. MDS-related BD shows distinctive characteristics [2,3], notably cytogenetic abnormalities such as trisomy 8 in bone marrow cells. Especially in Korea and Japan, bone marrow failure is frequently reported in patients with BD, and the proportion with trisomy 8 is strikingly high (63.6% to 86.0%) [2,3]. Clinically, BD patients with MDS have lower leukocyte counts, hemoglobin levels, and platelet counts and significantly higher levels of serum C-reactive protein and frequencies of intestinal BD than do BD patients without MDS. That is, patients with both BD and MDS have higher levels of disease activity than do BD patients without MDS. As a result, patients with MDS-related BD may be treated more frequently with corticosteroids and other immunosuppressive agents in various combinations. However, the disease is often refractory to these treatments. Furthermore, the control of intestinal BD in association with MDS using immunosuppressive agents, such as prednisolone alone, is difficult, and many patients die due to infection or hemorrhage. More encouraging are recent reports of successful treatment of MDS-related BD using HSCT. The positive response of the disorder to HSCT may plausibly occur through immunological reconstruction. A very grave risk to consider in treating MDS-related BD with HSCT is the induction of gastrointestinal GVHD. However, no reports to date have indicated that life-threatening gastrointestinal effects develop in patients treated with HSCT, including in our patient. In addition, patients with gastrointestinal disease before HSCT do not show an increased risk of gastrointestinal GVHD after treatment. Autologous HSCT even improves intestinal BD that was refractory to medical therapy [5].
In conclusion, BD may accompany MDS, possibly as an expression of a cytogenetic abnormality such as trisomy 8. A high frequency of intestinal BD with high disease activity is observed in MDS-related BD, and the intestinal disease may be refractory to therapy. HSTC presents a potentially effective treatment for MDS-related BD intractable to medical therapy without increasing the risk of gut GVHD. Further study of this treatment approach is justified.

Conflict of interest

No potential conflict of interest relevant to this article is reported.

References

1. Voulgarelis M, Giannouli S, Ritis K, Tzioufas AG. Myelodysplasia-associated autoimmunity: clinical and pathophysiologic concepts. Eur J Clin Invest 2004;34:690–700PMID : 15473894.
crossref pmid
2. Kawabata H, Sawaki T, Kawanami T, et al. Myelodysplastic syndrome complicated with inf lammatory intestinal ulcers: significance of trisomy 8. Intern Med 2006;45:1309–1314PMID : 17170506.
crossref pmid
3. Ahn JK, Cha HS, Koh EM, et al. Behcet's disease associated with bone marrow failure in Korean patients: clinical characteristics and the association of intestinal ulceration and trisomy 8. Rheumatology (Oxford) 2008;47:1228–1230PMID : 18550640.
crossref pmid
4. International Study Group for Behcet's Disease. Criteria for diagnosis of Behcet's disease. Lancet 1990;335:1078–1080PMID : 1970380.
pmid
5. Rossi G, Moretta A, Locatelli F. Autologous hematopoietic stem cell transplantation for severe/refractory intestinal Behcet disease. Blood 2004;103:748–750PMID : 14702292.
crossref pmid
Figure 1
(A) Friable erythematous mucosa and edematous shallow ulceration with irregular margins were observed at the ileocecal valve. (B) Marked improvement in the previous ulcerative lesion was noted at the ileocecal valve. Only a small ulceration remained.
kjim-29-123-g001
Figure 2
Pathologic examination of the colon reveals ulceration with glandular distortion, widening of the distance between the crypts, and prominent infiltration of inf lammatory cells, compatible with Behcet colitis (H&E, × 100).
kjim-29-123-g002
Editorial Office
101-2501, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea
Tel: +82-2-2271-6792   Fax: +82-2-790-0993    E-mail: kaim@kams.or.kr
Copyright © 2018 The Korean Association of Internal Medicine. All rights reserved.
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
powerd by m2community