Graft-Versus-Host Disease

Bone Marrow Transplantation (2005) 35, 91–97. doi:10.1038/sj.bmt.1704740 Published online 1 November 2004

Disseminated tuberculosis following reduced-intensity cord blood transplantation for adult patients with hematological diseases

T Maeda1, E Kusumi1, M Kami2, M Kawabata3, A Le Pavoux4, S Hara5, A Chizuka2, N Murashige2, T E Tanimoto6, T Matsumura1, Ko Yuji1, A Wake1, S Miyakoshi1, S Morinaga1 and S Taniguchi1 for the Tokyo Stem Cell Transplant (SCT) Consortium

  1. 1Department of Hematology, Toranomon Hospital, Tokyo, Japan
  2. 2Hematopoietic Stem Cell Transplant Unit, the National Cancer Center Hospital, Tokyo, Japan
  3. 3Department of Respiratory Medicine, Respiratory Center, Toranomon Hospital, Tokyo, Japan
  4. 4Department of Dermatology, Toranomon Hospital, Tokyo, Japan
  5. 5Department of Pathology, Toranomon Hospital, Tokyo, Japan
  6. 6First Department of Internal Medicine, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

Correspondence: Dr E Kusumi, Department of Hematology, Toranomon Hospital, 2-2-2, Toranomon, Minato-ku, Tokyo 105-8470, Japan. E-mail: kusumi-tora@umin.ac.jp

Received 8 August 2004; Accepted 7 September 2004; Published online 1 November 2004.

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Abstract

Allogeneic hematopoietic stem cell transplantation (allo-SCT) recipients are prone to infections. The incidences of mycobacterial infections after allo-SCT in several case series vary from less than 0.1–5.5%. However, no study has been published on tuberculosis following unrelated cord blood transplantation (UCBT). We retrospectively reviewed medical records of 113 adult patients with a median age of 54 years who underwent reduced-intensity UCBT (RI-UCBT) at Toranomon Hospital from March 2002 to May 2004. Mycobacterium tuberculosis infections were diagnosed in three patients (2.7%), of these two patients developed primary infection and one patient developed reactivation of latent tuberculosis. The interval between RI-UCBT and the diagnosis of tuberculosis was 34, 41 and 61 days. All the patients had disseminated disease at diagnosis. Histological examination showed the lack of granuloma in caseous necrosis. Combination antituberculous treatments showed limited efficacy, and two patients died immediately after diagnosis. M. tuberculosis caused life-threatening illness, rapidly progressing in RI-UCBT recipients. The lack of granuloma in caseous necrosis suggests the impaired T-cell function in early post transplant phase of RI-UCBT. We should consider M. tuberculosis in the differential diagnoses of fever of unknown source after RI-UCBT.

Keywords:

Mycobacterium tuberculosis, caseous necrosis, miliary tuberculosis, nonmyeloablative hematopoietic stem cell transplantation

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