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Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis

BACKGROUND: Cardinal criteria proposed by the World Health Organisation (WHO) lack sensitivity to diagnose indeterminate leprosy. AIMS: To estimate the frequency of hypopigmented skin lesions with doubtful/minimal sensory impairment showing histopathology features of indeterminate leprosy. To compar...

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Autores principales: Sasidharanpillai, Sarita, Govindan, Aparna, Dominic, Swapna, Binitha, Tattvamasi, Nandakumar, Veena, Devi, Keerankulangara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650743/
https://www.ncbi.nlm.nih.gov/pubmed/36386740
http://dx.doi.org/10.4103/idoj.idoj_114_22
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author Sasidharanpillai, Sarita
Govindan, Aparna
Dominic, Swapna
Binitha, Tattvamasi
Nandakumar, Veena
Devi, Keerankulangara
author_facet Sasidharanpillai, Sarita
Govindan, Aparna
Dominic, Swapna
Binitha, Tattvamasi
Nandakumar, Veena
Devi, Keerankulangara
author_sort Sasidharanpillai, Sarita
collection PubMed
description BACKGROUND: Cardinal criteria proposed by the World Health Organisation (WHO) lack sensitivity to diagnose indeterminate leprosy. AIMS: To estimate the frequency of hypopigmented skin lesions with doubtful/minimal sensory impairment showing histopathology features of indeterminate leprosy. To compare between the histopathology findings noted in specimens showing features suggestive of indeterminate leprosy and those showing a non-specific dermatitis pattern. MATERIALS AND METHODS: Data on patients who attended our department with hypopigmented patches with doubtful/minimal sensory impairment from January 2018 to December 2019 and who underwent a skin biopsy were collected. A pathologist blinded to the clinical findings reviewed the histopathology specimens using a pre-set questionnaire. RESULTS: We studied sixteen biopsy specimens from 14 patients. Eight specimens (50%) showed histopathology suggestive of indeterminate leprosy and the remaining eight showed a non-specific dermatitis pattern. A higher percentage of patients with indeterminate pattern showed mast cells (87.5% vs 25%) and fibrosis around nerve twig or sweat duct (75% vs 12.5%) when compared to those who showed a non-specific dermatitis pattern. LIMITATIONS: Small sample size and retrospective study design were the limitations. CONCLUSIONS: We found histopathology features of indeterminate leprosy in 50% of the skin biopsy specimens from hypopigmented lesions with doubtful/minimal sensory impairment. The present study highlights the need to improve the diagnostic definition of indeterminate leprosy.
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spelling pubmed-96507432022-11-15 Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis Sasidharanpillai, Sarita Govindan, Aparna Dominic, Swapna Binitha, Tattvamasi Nandakumar, Veena Devi, Keerankulangara Indian Dermatol Online J Brief Report BACKGROUND: Cardinal criteria proposed by the World Health Organisation (WHO) lack sensitivity to diagnose indeterminate leprosy. AIMS: To estimate the frequency of hypopigmented skin lesions with doubtful/minimal sensory impairment showing histopathology features of indeterminate leprosy. To compare between the histopathology findings noted in specimens showing features suggestive of indeterminate leprosy and those showing a non-specific dermatitis pattern. MATERIALS AND METHODS: Data on patients who attended our department with hypopigmented patches with doubtful/minimal sensory impairment from January 2018 to December 2019 and who underwent a skin biopsy were collected. A pathologist blinded to the clinical findings reviewed the histopathology specimens using a pre-set questionnaire. RESULTS: We studied sixteen biopsy specimens from 14 patients. Eight specimens (50%) showed histopathology suggestive of indeterminate leprosy and the remaining eight showed a non-specific dermatitis pattern. A higher percentage of patients with indeterminate pattern showed mast cells (87.5% vs 25%) and fibrosis around nerve twig or sweat duct (75% vs 12.5%) when compared to those who showed a non-specific dermatitis pattern. LIMITATIONS: Small sample size and retrospective study design were the limitations. CONCLUSIONS: We found histopathology features of indeterminate leprosy in 50% of the skin biopsy specimens from hypopigmented lesions with doubtful/minimal sensory impairment. The present study highlights the need to improve the diagnostic definition of indeterminate leprosy. Wolters Kluwer - Medknow 2022-07-18 /pmc/articles/PMC9650743/ /pubmed/36386740 http://dx.doi.org/10.4103/idoj.idoj_114_22 Text en Copyright: © 2022 Indian Dermatology Online Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Brief Report
Sasidharanpillai, Sarita
Govindan, Aparna
Dominic, Swapna
Binitha, Tattvamasi
Nandakumar, Veena
Devi, Keerankulangara
Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title_full Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title_fullStr Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title_full_unstemmed Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title_short Hypopigmented Skin Lesions with Doubtful/Minimal Sensory Impairment: A Histopathology-Based Analysis
title_sort hypopigmented skin lesions with doubtful/minimal sensory impairment: a histopathology-based analysis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9650743/
https://www.ncbi.nlm.nih.gov/pubmed/36386740
http://dx.doi.org/10.4103/idoj.idoj_114_22
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