Oral tuberculosis following autologous bone marrow transplantation for Hodgkin's disease with interleukin-2 and α-interferon immunotherapy

A. Toren; A. Ackerstein; D. Gazit; R. Or; D. Raveh; U. Kupolovicz; D. Engelhard; A. Nagler

Oral tuberculosis following autologous bone marrow transplantation for Hodgkin's disease with interleukin-2 and α-interferon immunotherapy

A. Toren
, A. Ackerstein
, D. Gazit
, R. Or
, D. Raveh
, U. Kupolovicz
, D. Engelhard
, A. Nagler^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Abstract

A patient with Hodgkin's disease (HD) underwent autologous bone marrow transplantation (ABMT). Six months later while receiving interleukin (IL)-2 and α-interferon immunotherapy, he developed a painful lesion in his oral cavity with a fistula in the buccal area. Excision biopsy disclosed necrotizing granulomatous inflammation with acid-fast bacillus. The patient received a 9-month course of isoniazide, rifampin and pyranizamide, and recovered. The possible pathophysiological mechanism is discussed.

Original language	English
Pages (from-to)	209-210
Number of pages	2
Journal	Bone Marrow Transplantation
Volume	18
Issue number	1
State	Published - Jul 1996
Externally published	Yes

Keywords

Autologous bone marrow transplantation
Immunotherapy
Tuberculosis

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This output contributes to the following UN Sustainable Development Goals (SDGs)

Cite this

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title = "Oral tuberculosis following autologous bone marrow transplantation for Hodgkin's disease with interleukin-2 and α-interferon immunotherapy",

abstract = "A patient with Hodgkin's disease (HD) underwent autologous bone marrow transplantation (ABMT). Six months later while receiving interleukin (IL)-2 and α-interferon immunotherapy, he developed a painful lesion in his oral cavity with a fistula in the buccal area. Excision biopsy disclosed necrotizing granulomatous inflammation with acid-fast bacillus. The patient received a 9-month course of isoniazide, rifampin and pyranizamide, and recovered. The possible pathophysiological mechanism is discussed.",

keywords = "Autologous bone marrow transplantation, Immunotherapy, Tuberculosis",

author = "A. Toren and A. Ackerstein and D. Gazit and R. Or and D. Raveh and U. Kupolovicz and D. Engelhard and A. Nagler",

year = "1996",

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T1 - Oral tuberculosis following autologous bone marrow transplantation for Hodgkin's disease with interleukin-2 and α-interferon immunotherapy

AU - Toren, A.

AU - Ackerstein, A.

AU - Gazit, D.

AU - Or, R.

AU - Raveh, D.

AU - Kupolovicz, U.

AU - Engelhard, D.

AU - Nagler, A.

PY - 1996/7

Y1 - 1996/7

N2 - A patient with Hodgkin's disease (HD) underwent autologous bone marrow transplantation (ABMT). Six months later while receiving interleukin (IL)-2 and α-interferon immunotherapy, he developed a painful lesion in his oral cavity with a fistula in the buccal area. Excision biopsy disclosed necrotizing granulomatous inflammation with acid-fast bacillus. The patient received a 9-month course of isoniazide, rifampin and pyranizamide, and recovered. The possible pathophysiological mechanism is discussed.

AB - A patient with Hodgkin's disease (HD) underwent autologous bone marrow transplantation (ABMT). Six months later while receiving interleukin (IL)-2 and α-interferon immunotherapy, he developed a painful lesion in his oral cavity with a fistula in the buccal area. Excision biopsy disclosed necrotizing granulomatous inflammation with acid-fast bacillus. The patient received a 9-month course of isoniazide, rifampin and pyranizamide, and recovered. The possible pathophysiological mechanism is discussed.

KW - Autologous bone marrow transplantation

KW - Immunotherapy

KW - Tuberculosis

UR - https://www.scopus.com/pages/publications/0029775180

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AN - SCOPUS:0029775180

SN - 0268-3369

VL - 18

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EP - 210

JO - Bone Marrow Transplantation

JF - Bone Marrow Transplantation

IS - 1

ER -

Oral tuberculosis following autologous bone marrow transplantation for Hodgkin's disease with interleukin-2 and α-interferon immunotherapy

Abstract

Keywords

UN SDGs

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