Cargando…

Single lesion multibacillary leprosy, a treatment enigma: a case report

INTRODUCTION: Leprosy exhibits a wide spectrum of presentation, varying from the tuberculoid to the lepromatous pole, with immunologically unstable borderline forms in-between, depending upon the immune status of the individual. The clinical system of classification for the purpose of treatment incl...

Descripción completa

Detalles Bibliográficos
Autores principales: Sapkota, Bishwa R, Neupane, Kapil D, Maharjan, Ram K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628938/
https://www.ncbi.nlm.nih.gov/pubmed/19144101
http://dx.doi.org/10.1186/1752-1947-3-8
_version_ 1782163756335235072
author Sapkota, Bishwa R
Neupane, Kapil D
Maharjan, Ram K
author_facet Sapkota, Bishwa R
Neupane, Kapil D
Maharjan, Ram K
author_sort Sapkota, Bishwa R
collection PubMed
description INTRODUCTION: Leprosy exhibits a wide spectrum of presentation, varying from the tuberculoid to the lepromatous pole, with immunologically unstable borderline forms in-between, depending upon the immune status of the individual. The clinical system of classification for the purpose of treatment includes the number of skin lesions and nerves involved as the basis for classifying the patients into multibacillary and paucibacillary. CASE PRESENTATION: A 20-year-old man belonging to a moderately endemic leprosy area in the Terai region of Nepal reported a large single, hypopigmented, well defined anaesthetic lesion on his left thigh extending to his knee which had been present for 2 years. There was no other nerve involvement. Clinical diagnosis was tuberculoid leprosy and immunological lateral flow test for anti-Phenolic glycolipid-I antibody was positive. Six months of paucibacillary multidrug treatment was advised immediately. However, the patient was reclassified as multibacillary on the basis of a positive skin smear and appropriate treatment of 24 months multibacillary multidrug regimen was commenced after only 1 week. Slit skin smear examination for Mycobacterium leprae from the lesion revealed a bacterial index of 4+ while it was negative from the routine sites. Histopathological examination from skin biopsy of the lesion further supported the bacterial index of the lesion granuloma which was 2+ and the patient was diagnosed as borderline tuberculoid. Bacteriological, histological, and immunological findings of this patient were borderline tuberculoid leprosy and he should have been treated with multibacillary regimen from the beginning. Five months after commencement of treatment, the patient developed a leprae reaction of Type 1 or reversal reaction with some nerve function impairment and enlargement of the lateral popliteal nerve of the left leg. This reversal reaction was managed by standard oral prednisolone whilst continuing the multibacillary multidrug regimen. CONCLUSION: This case illustrates and emphasizes the importance of slit-skin smear and biopsy as routine in all new cases to help differentiate multibacillary from paucibacillary for correct treatment. It further suggests that there are factors yet undetermined which play a significant role in determining the host response to M. leprae which is a remaining challenge in this disease.
format Text
id pubmed-2628938
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26289382009-01-21 Single lesion multibacillary leprosy, a treatment enigma: a case report Sapkota, Bishwa R Neupane, Kapil D Maharjan, Ram K J Med Case Reports Case report INTRODUCTION: Leprosy exhibits a wide spectrum of presentation, varying from the tuberculoid to the lepromatous pole, with immunologically unstable borderline forms in-between, depending upon the immune status of the individual. The clinical system of classification for the purpose of treatment includes the number of skin lesions and nerves involved as the basis for classifying the patients into multibacillary and paucibacillary. CASE PRESENTATION: A 20-year-old man belonging to a moderately endemic leprosy area in the Terai region of Nepal reported a large single, hypopigmented, well defined anaesthetic lesion on his left thigh extending to his knee which had been present for 2 years. There was no other nerve involvement. Clinical diagnosis was tuberculoid leprosy and immunological lateral flow test for anti-Phenolic glycolipid-I antibody was positive. Six months of paucibacillary multidrug treatment was advised immediately. However, the patient was reclassified as multibacillary on the basis of a positive skin smear and appropriate treatment of 24 months multibacillary multidrug regimen was commenced after only 1 week. Slit skin smear examination for Mycobacterium leprae from the lesion revealed a bacterial index of 4+ while it was negative from the routine sites. Histopathological examination from skin biopsy of the lesion further supported the bacterial index of the lesion granuloma which was 2+ and the patient was diagnosed as borderline tuberculoid. Bacteriological, histological, and immunological findings of this patient were borderline tuberculoid leprosy and he should have been treated with multibacillary regimen from the beginning. Five months after commencement of treatment, the patient developed a leprae reaction of Type 1 or reversal reaction with some nerve function impairment and enlargement of the lateral popliteal nerve of the left leg. This reversal reaction was managed by standard oral prednisolone whilst continuing the multibacillary multidrug regimen. CONCLUSION: This case illustrates and emphasizes the importance of slit-skin smear and biopsy as routine in all new cases to help differentiate multibacillary from paucibacillary for correct treatment. It further suggests that there are factors yet undetermined which play a significant role in determining the host response to M. leprae which is a remaining challenge in this disease. BioMed Central 2009-01-13 /pmc/articles/PMC2628938/ /pubmed/19144101 http://dx.doi.org/10.1186/1752-1947-3-8 Text en Copyright ©2009 Sapkota et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case report
Sapkota, Bishwa R
Neupane, Kapil D
Maharjan, Ram K
Single lesion multibacillary leprosy, a treatment enigma: a case report
title Single lesion multibacillary leprosy, a treatment enigma: a case report
title_full Single lesion multibacillary leprosy, a treatment enigma: a case report
title_fullStr Single lesion multibacillary leprosy, a treatment enigma: a case report
title_full_unstemmed Single lesion multibacillary leprosy, a treatment enigma: a case report
title_short Single lesion multibacillary leprosy, a treatment enigma: a case report
title_sort single lesion multibacillary leprosy, a treatment enigma: a case report
topic Case report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2628938/
https://www.ncbi.nlm.nih.gov/pubmed/19144101
http://dx.doi.org/10.1186/1752-1947-3-8
work_keys_str_mv AT sapkotabishwar singlelesionmultibacillaryleprosyatreatmentenigmaacasereport
AT neupanekapild singlelesionmultibacillaryleprosyatreatmentenigmaacasereport
AT maharjanramk singlelesionmultibacillaryleprosyatreatmentenigmaacasereport