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Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1377
Study of Histomorphological Spectrum of
Lesions in Leprosy- One Year Study in S N
Medical College, Bagalkote
Anusha KS1
, Prabhu MH2*
, Dombale VD3
1
Assistant Professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote, Karnataka, India
2
Associate professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote Karnataka, India
3
Professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote, Karnataka, India
*
Address for Correspondence: Dr. Prabhu M H, Associate Professor, Department of Pathology, S. N. Medical
College, Navnagar, Bagalkote- 587103, India
Received: 06 June 2017/Revised: 28 July 2017/Accepted: 22 August 2017
ABSTRACT- Introduction: Leprosy one of the oldest and chronic infectious disease caused by Mycobacterium
leprae. Leprosy is widely prevalent in India. Most of the cases present as hypopigmented patches or erythematous
lesions over skin. However on histopathology these lesions show a wide spectrum of changes and variations.
Material And Methods: A retrospective study of diagnosed cases of leprosy on skin biopsy in Department of
Pathology, S Nijalingappa Medical College from January 2015 to January 2016. Total of 63 cases were re-evaluated
and classified according to Ridley-Jopling classification.
Results: Lesions were most oftenly seen in middle aged patients and most common symptom was hypopigmented patch
(68.2%). Based on Ridley-Jopling classification, most cases were lepromatous leprosy (23.8%) followed by borderline
lepromatous type (22.2%), indeterminate type (22.2%), tuberculoid leprosy (6.3%), borderline tuberculoid leprosy
(17.4%) and borderline borderline leprosy (7.9%). Wade-Fite staining was done in 42 cases out of which 17 cases
showed positive for acid-fast bacilli. Also noted that the bacilli load was >2+ in lepromatous spectrum.
Conclusion: Histopathology remains the important tool to diagnose the subtype of leprosy lesions. Lepromatous
leprosy is most often associated with high bacterial load.
Key-words- Histomorphological Spectrum, Lepromatous spectrum, Mycobacterium leprae, Leprosy
INTRODUCTION
Leprosy is a chronic granulomatous infection caused by
Mycobacterium leprae. It is also known as Hansen’s
disease. M. leprae commonly affects the skin and
peripheral nerves.[1]
It can also involve muscles, eyes,
bones, testis and internal organs.[2]
Diagnosis of leprosy
can be done by clinical, microbiological and
histopathological examination which includes, detail
examination of skin lesions and peripheral nerves,
demonstration of lepra bacilli by Fite’s acid fast stain in
slit skin smears and histopathological diagnosis and
demonstration of bacilli in histopathological sections.[3]
Though most cases of leprosy can be diagnosed clinically
without histopathological examination, it is still
considered as important test for confirmatory diagnosis,
for assessment of regression of the disease in patient
under treatment and also for research purposes.
Access this article online
Quick Response Code Website:
www.ijlssr.com
DOI: 10.21276/ijlssr.2017.3.5.19
Interaction between pathologist and dermatologist may be
beneficial for proper diagnosis and management of the
patient.[4]
The principle of reducing the load of infection is the
cornerstone of leprosy control by early diagnosis and
early adequate drug treatment. So confirmation of
diagnosis in doubtful cases is an important indication for
histopathological examination.[5]
The disease spectrum has been characterised in a number
of classification systems, most widely being the
Ridley-Jopling classification. In this classification,
leprosy has been divided into five groups as Tuberculoid
(TT), Borderline tuberculoid (BT), Mid-bordrline (BB),
Borderline Lepromatous (BL), and Lepromatous (LL).[6]
The Classification has been accepted worldwide and is
highly recommended. Though the clinical diagnosis is
based on characteristic skin lesions with sensory loss, a
great variation is seen in interpretation of these lesions,
both clinically and histopathologically.[7]
MATERIALS AND METHODS
It was a retrospective study from January 2015 to January
2016 in Department of Pathology, S Nijalingappa
Medical College, Karnataka, India. We commonly
received cone biopsy specimens of clinically suspected
RESEARCH ARTICLE
Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1378
cases of leprosy. The specimens were routinely processed
and sectioned; slides were stained with haematoxylin and
eosin. Extra sections were taken and also stained with
Wade-Fite stain in order to demonstrate acid-fast bacilli.
The bacillary index was calculated based on the criteria
given in Table 1. Histopathological evaluation included
invasion of epidermis, involvement of sub-epidermal
zone, character & extent of granulomas, density of
lymphocytic infiltrate, epitheloid cells and other cellular
elements, nerve involvement and presence of M. leprae.
RESULTS
Total of 63 cases were re-evaluated and classified
according to Ridley-Jopling classification. Out of 63
cases 40 were males and 23 females. The age of the
patients ranged from 10 to 80 years. Majority of patients
belonged to the age group of 30-45 years. Based on
Ridley-Jopling classification the cases were divided into
six groups.
Table 1: Grading of Bacillary load according to
Bacillary Index criteria
Grade Bacilli Examine OIF
1+ 1-10 bacilli in 100 OIF 100 OIF
2+ 0 1-10 bacilli in 10 OIF 100 OIF
3+ 1-10 bacilli in 1 OIF 25 OIF
4+ 10-100 bacilli in 1 OIF 25 OIF
5+ 100-1000 bacilli in 1 OIF 25 OIF
6+ ≥1000 bacilli in 1 OIF 25 OIF
Table 2: Distribution of cases based on Ridley Jopling
Classification
Type of Leprosy No. of cases Percentage (%)
Tuberculoid 04 6.3
Borderline
tuberculoid
11 17.4
Mid Borderline 05 7.9
Borderline
lepromatous
14 22.2
Lepromatous 15 23.8
Indeterminate 14 22.2
Lepromatous leprosy were most common identified type
of leprosy constituting 15 cases followed by 14 cases of
each of mid-borderline and indeterminate cases.
Fig. 1: Distribution of cases represented in a Pie chart
Out of 63 cases 24 turned positive for acid fast bacilli on
Wade-Fite staining.
Table 3: Acid-fast Bacilli (AFB) Positive cases in
various Leprosy lesions on Wade Fite staining
Histological type of
leprosy
Positive
cases
Negative
cases
Percentage
Tuberculoid - 04 -
Boderline
Tuberculoid
- 11 -
Borderline
Borderline
03 02 60%
Borderline
Lepromatous
06 08 42.8%
Lepromatous 12 03 80%
Indeterminate 03 11 21.4%
Total=24 Total=39
The changes in epidermis comprised of epithelial
hyperplasia, atrophy and spongiosis. The commonest
change was atrophy of epidermis.
Table 4: Changes in Histopathology of Epidermis in
Leprosy lesions
Histopathology
of epidermis
Tuberculoid
Group
Inderminate
Group
Lepromatous
Group
No change 2 3 2
Hyperplasia 1 2 -
Atrophy 17 7 23
Spongiosis - 2 4
N=20 N=14 N=29
Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1379
The dermal changes include presence of Grenz zone, diffuse infiltrate of inflammatory cells, changes in arrector pili
muscle (no change, inflammation, atrophy), sweat glands (no change/inflammation), hair follicles (no change or
inflammation), perineural inflammation were observed in tuberculoid, indeterminate and lepromatous group of leprosy
lesions.
Table 5: Changes in Histopathology of Dermis in Leprosy leions
Histopathology of Dermis Tuberculoid
N=20
Indeterminate
N=14
Lepromatous
N=29
Grenz Zone 5 8 21
Diffuse infiltrate of
inflammatory cells
12 6 25
Arrector pili muscle
No change 10 13 3
Inflammation 8 1 23
Atrophy 2 - 3
Sweat glands
No change 9 12 10
Inflammation 11 2 19
Hair follicles
No change - - 4
Inflammation 12 2 23
Atrophy - - -
Not demonstrable 8 12 2
Cutaneous nerves
No change - 13 -
Perineural inflammation 7 1 21
Infiltration within the nerve 2 - 8
Not demonstrable 11 - -
Perineural inflammation was seen in total of 29 cases and infiltration of inflammatory cell within the nerve was seen in
10 cases.
Table 6: Comparison of the present study results with other studies
Studies Total no.
of cases
Year TT BT BB BL LL IL
Mistry et al. [8]
59 2015 17.24% 27.14% 6.45% 29.03% 9.46% 5.08%
Murthy et al. [5]
100 2015 1% 57% 0% 2% 11% 9%
Sharma et al. [3]
247 2008 8.09% 35.2% 18.2% 6.4% 10.1% 21.8%
Chauhari et al.
[9]
126 2012 26.6% 13.3% 3.3% 23.3% 33.3% -
Present study 63 2015 6.3% 17.4% 7.9% 22.2% 23.8% 22.2%
Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1380
Fig. 2 (a): Tuberculoid leprosy showing well formed granulomas (scanner view)
(b) Borderline tuberculoid leprosy breeching epidermis (40X)
(c) Mid- borderline case (10X)
(d) Micrograph showing perineural lymphocytic infiltration in a case of Leprosy (10X)
(e) Histioid leprosy showing sheets of macrophages (10X)
(f) Clumps of lepra bacilli on Wade-Fite staining (100X)
DISCUSSION
Leprosy is a chronic granulomatous lesion leading to
various skin lesions. In our study the disease is common
in male when compared to females in concordance with
various other studies. Majority of patients presented with
hypopigmented patches and few presentations of
erythematous patch and nodules also noted.
The commonest type in our study is lepromatous leprosy
in concordant with the study done by Chauhari et al. [9]
.
In study done by Sharma et al. [3]
, borderline tuberculoid
was the commonest type, where as it constituted only
17.4% in our study.
In study done by Mistry et al. [8]
, studied 59 cases of
leprosy, out of which 28 patients were on tuberculoid
pole (lymphocyte predominant infiltrate) and 32 patients
were on lepromatous pole (macrophage predominant
infiltrate) [8]
whereas in our study 20 were on the
tuberculoid pole and 29 were on lepromatous pole. The
various clinical forms by which leprosy establishes are
complemented by particular histopathological picture.
Thus, histopathology reveals epithelioid cells, Langhans
giant cells, and lymphocytes in toward the TT end of the
spectrum and while foamy macrophages are abundant
toward LL end of spectrum.
According to Murthy et al. [5]
, the correlation without
immunological assessment can never be 100%. But
properly applied, with the three parameters alone namely,
clinical, bacteriological and histological about 50-80%
correlations can be achieved. Histopathological study in
this series has certainly raised awareness, in that some of
the clinically tuberculoid cases showed definite LL
change thereby giving a warning to undertake careful
follow up. All clinically diagnosed Hansen’s disease
should be submitted to histopathology whenever possible,
so that it will help in determining the type of the disease
and duration of treatment.
CONCLUSIONS
Leprosy has wide morphological spectrum.
Histopathology is helpful for typing of leprosy specially
using Ridley-Jopling classification. Lepromatous leprosy
is the commonest type and need to be carefully reported.
Demonstration of acid fast bacilli yields better report as
well as helps the treatment plan according to national
leprosy programmes. Histopathology and demonstration
of bacilli collectively helps in planning the appropriate
treatment.
Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017
Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1381
REFERENCES
[1] Tiwari M, Ranabhat S, Maharjan S.
Clinico-histopathological correlation of leprosy: A
retrospective study of skin biopsy specimens in Chitwan
Medical College. International Journal of Medical Science
Research and Practice 2015; 2(1):8-11.
[2] Park JE, Park K. Epidemiology of communicable diseases.
In: Preventive and Social Medicine. Jabalpur: Banarasidas
Bhanol; 1991. p. 215-25.
[3] Sharma A, Kumar RS, Goswsami CK, Bardwaj S.
Clinicohistopathological correlation in leprosy. JK Sci
2008; 10:120-3.
[4] Manandhar U, Adhikari RC, Sayami G.
Clinico-histopathological correlation of skin biopsies in
leprosy. J Pathol Nepal 2013; 3:452-8.
[5] Murthy M. Suryanarayana, Gitu Duara, K. Kasi
Viswanath, Kiran Kanth. Clinical and Histopathological
Correlation in Hansen’s Disease. Journal of Evolution of
Medical and Dental Sciences 2015; 4(35): 6081-6085.
[6] Mathur MC, Ghimire RBK, Shrestha P, Kedia SK.
Clinicohistopathological Correlation in Leprosy.
Kathmandu Univ Med J. 2011; 36(4):248-51.
[7] Giridhar M, Arora G, Lajpal K, Chahal KS.
Clinicohistopathological concordance in Leprosy- A
Clinical, Histopathological and Bacteriological study of
100 cases. Indian J Lepr 2012; 84:217-25.
[8] Mistry A S, Rathod S P, Agarwal P. An institution-based
observational study to identify sensitive histopathological
parameters in leprosy. 2015; 4(12):1720-25
[9] Chauhari B, Mehta RP. Clinico-histopathological
correlation in Leprosy. International Journal of Scientific
Research, 2012;1(5): 104-105.
International Journal of Life Sciences Scientific Research (IJLSSR)
Open Access Policy
Authors/Contributors are responsible for originality, contents, correct
references, and ethical issues.
IJLSSR publishes all articles under Creative Commons
Attribution- Non-Commercial 4.0 International License (CC BY-NC).
https://creativecommons.org/licenses/by-nc/4.0/legalcode
How to cite this article:
Anusha KS, Prabhu MH, Dombale VD: Study of Histomorphological Spectrum of Lesions in Leprosy- One Year Study in S
N Medical College, Bagalkote. Int. J. Life. Sci. Scienti. Res., 2017; 3(5):1377-1381. DOI:10.21276/ijlssr.2017.3.5.19
Source of Financial Support: Nil, Conflict of interest: Nil

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Histopathological Spectrum of Leprosy Lesions

  • 1. Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1377 Study of Histomorphological Spectrum of Lesions in Leprosy- One Year Study in S N Medical College, Bagalkote Anusha KS1 , Prabhu MH2* , Dombale VD3 1 Assistant Professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote, Karnataka, India 2 Associate professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote Karnataka, India 3 Professor, Dept. of Pathology, S. Nijalingappa Medical College, Bagalkote, Karnataka, India * Address for Correspondence: Dr. Prabhu M H, Associate Professor, Department of Pathology, S. N. Medical College, Navnagar, Bagalkote- 587103, India Received: 06 June 2017/Revised: 28 July 2017/Accepted: 22 August 2017 ABSTRACT- Introduction: Leprosy one of the oldest and chronic infectious disease caused by Mycobacterium leprae. Leprosy is widely prevalent in India. Most of the cases present as hypopigmented patches or erythematous lesions over skin. However on histopathology these lesions show a wide spectrum of changes and variations. Material And Methods: A retrospective study of diagnosed cases of leprosy on skin biopsy in Department of Pathology, S Nijalingappa Medical College from January 2015 to January 2016. Total of 63 cases were re-evaluated and classified according to Ridley-Jopling classification. Results: Lesions were most oftenly seen in middle aged patients and most common symptom was hypopigmented patch (68.2%). Based on Ridley-Jopling classification, most cases were lepromatous leprosy (23.8%) followed by borderline lepromatous type (22.2%), indeterminate type (22.2%), tuberculoid leprosy (6.3%), borderline tuberculoid leprosy (17.4%) and borderline borderline leprosy (7.9%). Wade-Fite staining was done in 42 cases out of which 17 cases showed positive for acid-fast bacilli. Also noted that the bacilli load was >2+ in lepromatous spectrum. Conclusion: Histopathology remains the important tool to diagnose the subtype of leprosy lesions. Lepromatous leprosy is most often associated with high bacterial load. Key-words- Histomorphological Spectrum, Lepromatous spectrum, Mycobacterium leprae, Leprosy INTRODUCTION Leprosy is a chronic granulomatous infection caused by Mycobacterium leprae. It is also known as Hansen’s disease. M. leprae commonly affects the skin and peripheral nerves.[1] It can also involve muscles, eyes, bones, testis and internal organs.[2] Diagnosis of leprosy can be done by clinical, microbiological and histopathological examination which includes, detail examination of skin lesions and peripheral nerves, demonstration of lepra bacilli by Fite’s acid fast stain in slit skin smears and histopathological diagnosis and demonstration of bacilli in histopathological sections.[3] Though most cases of leprosy can be diagnosed clinically without histopathological examination, it is still considered as important test for confirmatory diagnosis, for assessment of regression of the disease in patient under treatment and also for research purposes. Access this article online Quick Response Code Website: www.ijlssr.com DOI: 10.21276/ijlssr.2017.3.5.19 Interaction between pathologist and dermatologist may be beneficial for proper diagnosis and management of the patient.[4] The principle of reducing the load of infection is the cornerstone of leprosy control by early diagnosis and early adequate drug treatment. So confirmation of diagnosis in doubtful cases is an important indication for histopathological examination.[5] The disease spectrum has been characterised in a number of classification systems, most widely being the Ridley-Jopling classification. In this classification, leprosy has been divided into five groups as Tuberculoid (TT), Borderline tuberculoid (BT), Mid-bordrline (BB), Borderline Lepromatous (BL), and Lepromatous (LL).[6] The Classification has been accepted worldwide and is highly recommended. Though the clinical diagnosis is based on characteristic skin lesions with sensory loss, a great variation is seen in interpretation of these lesions, both clinically and histopathologically.[7] MATERIALS AND METHODS It was a retrospective study from January 2015 to January 2016 in Department of Pathology, S Nijalingappa Medical College, Karnataka, India. We commonly received cone biopsy specimens of clinically suspected RESEARCH ARTICLE
  • 2. Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1378 cases of leprosy. The specimens were routinely processed and sectioned; slides were stained with haematoxylin and eosin. Extra sections were taken and also stained with Wade-Fite stain in order to demonstrate acid-fast bacilli. The bacillary index was calculated based on the criteria given in Table 1. Histopathological evaluation included invasion of epidermis, involvement of sub-epidermal zone, character & extent of granulomas, density of lymphocytic infiltrate, epitheloid cells and other cellular elements, nerve involvement and presence of M. leprae. RESULTS Total of 63 cases were re-evaluated and classified according to Ridley-Jopling classification. Out of 63 cases 40 were males and 23 females. The age of the patients ranged from 10 to 80 years. Majority of patients belonged to the age group of 30-45 years. Based on Ridley-Jopling classification the cases were divided into six groups. Table 1: Grading of Bacillary load according to Bacillary Index criteria Grade Bacilli Examine OIF 1+ 1-10 bacilli in 100 OIF 100 OIF 2+ 0 1-10 bacilli in 10 OIF 100 OIF 3+ 1-10 bacilli in 1 OIF 25 OIF 4+ 10-100 bacilli in 1 OIF 25 OIF 5+ 100-1000 bacilli in 1 OIF 25 OIF 6+ ≥1000 bacilli in 1 OIF 25 OIF Table 2: Distribution of cases based on Ridley Jopling Classification Type of Leprosy No. of cases Percentage (%) Tuberculoid 04 6.3 Borderline tuberculoid 11 17.4 Mid Borderline 05 7.9 Borderline lepromatous 14 22.2 Lepromatous 15 23.8 Indeterminate 14 22.2 Lepromatous leprosy were most common identified type of leprosy constituting 15 cases followed by 14 cases of each of mid-borderline and indeterminate cases. Fig. 1: Distribution of cases represented in a Pie chart Out of 63 cases 24 turned positive for acid fast bacilli on Wade-Fite staining. Table 3: Acid-fast Bacilli (AFB) Positive cases in various Leprosy lesions on Wade Fite staining Histological type of leprosy Positive cases Negative cases Percentage Tuberculoid - 04 - Boderline Tuberculoid - 11 - Borderline Borderline 03 02 60% Borderline Lepromatous 06 08 42.8% Lepromatous 12 03 80% Indeterminate 03 11 21.4% Total=24 Total=39 The changes in epidermis comprised of epithelial hyperplasia, atrophy and spongiosis. The commonest change was atrophy of epidermis. Table 4: Changes in Histopathology of Epidermis in Leprosy lesions Histopathology of epidermis Tuberculoid Group Inderminate Group Lepromatous Group No change 2 3 2 Hyperplasia 1 2 - Atrophy 17 7 23 Spongiosis - 2 4 N=20 N=14 N=29
  • 3. Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1379 The dermal changes include presence of Grenz zone, diffuse infiltrate of inflammatory cells, changes in arrector pili muscle (no change, inflammation, atrophy), sweat glands (no change/inflammation), hair follicles (no change or inflammation), perineural inflammation were observed in tuberculoid, indeterminate and lepromatous group of leprosy lesions. Table 5: Changes in Histopathology of Dermis in Leprosy leions Histopathology of Dermis Tuberculoid N=20 Indeterminate N=14 Lepromatous N=29 Grenz Zone 5 8 21 Diffuse infiltrate of inflammatory cells 12 6 25 Arrector pili muscle No change 10 13 3 Inflammation 8 1 23 Atrophy 2 - 3 Sweat glands No change 9 12 10 Inflammation 11 2 19 Hair follicles No change - - 4 Inflammation 12 2 23 Atrophy - - - Not demonstrable 8 12 2 Cutaneous nerves No change - 13 - Perineural inflammation 7 1 21 Infiltration within the nerve 2 - 8 Not demonstrable 11 - - Perineural inflammation was seen in total of 29 cases and infiltration of inflammatory cell within the nerve was seen in 10 cases. Table 6: Comparison of the present study results with other studies Studies Total no. of cases Year TT BT BB BL LL IL Mistry et al. [8] 59 2015 17.24% 27.14% 6.45% 29.03% 9.46% 5.08% Murthy et al. [5] 100 2015 1% 57% 0% 2% 11% 9% Sharma et al. [3] 247 2008 8.09% 35.2% 18.2% 6.4% 10.1% 21.8% Chauhari et al. [9] 126 2012 26.6% 13.3% 3.3% 23.3% 33.3% - Present study 63 2015 6.3% 17.4% 7.9% 22.2% 23.8% 22.2%
  • 4. Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1380 Fig. 2 (a): Tuberculoid leprosy showing well formed granulomas (scanner view) (b) Borderline tuberculoid leprosy breeching epidermis (40X) (c) Mid- borderline case (10X) (d) Micrograph showing perineural lymphocytic infiltration in a case of Leprosy (10X) (e) Histioid leprosy showing sheets of macrophages (10X) (f) Clumps of lepra bacilli on Wade-Fite staining (100X) DISCUSSION Leprosy is a chronic granulomatous lesion leading to various skin lesions. In our study the disease is common in male when compared to females in concordance with various other studies. Majority of patients presented with hypopigmented patches and few presentations of erythematous patch and nodules also noted. The commonest type in our study is lepromatous leprosy in concordant with the study done by Chauhari et al. [9] . In study done by Sharma et al. [3] , borderline tuberculoid was the commonest type, where as it constituted only 17.4% in our study. In study done by Mistry et al. [8] , studied 59 cases of leprosy, out of which 28 patients were on tuberculoid pole (lymphocyte predominant infiltrate) and 32 patients were on lepromatous pole (macrophage predominant infiltrate) [8] whereas in our study 20 were on the tuberculoid pole and 29 were on lepromatous pole. The various clinical forms by which leprosy establishes are complemented by particular histopathological picture. Thus, histopathology reveals epithelioid cells, Langhans giant cells, and lymphocytes in toward the TT end of the spectrum and while foamy macrophages are abundant toward LL end of spectrum. According to Murthy et al. [5] , the correlation without immunological assessment can never be 100%. But properly applied, with the three parameters alone namely, clinical, bacteriological and histological about 50-80% correlations can be achieved. Histopathological study in this series has certainly raised awareness, in that some of the clinically tuberculoid cases showed definite LL change thereby giving a warning to undertake careful follow up. All clinically diagnosed Hansen’s disease should be submitted to histopathology whenever possible, so that it will help in determining the type of the disease and duration of treatment. CONCLUSIONS Leprosy has wide morphological spectrum. Histopathology is helpful for typing of leprosy specially using Ridley-Jopling classification. Lepromatous leprosy is the commonest type and need to be carefully reported. Demonstration of acid fast bacilli yields better report as well as helps the treatment plan according to national leprosy programmes. Histopathology and demonstration of bacilli collectively helps in planning the appropriate treatment.
  • 5. Int. J. Life. Sci. Scienti. Res., 3(5): 1377-1381 SEPTEMBER 2017 Copyright © 2015-2017| IJLSSR by Society for Scientific Research is under a CC BY-NC 4.0 International License Page 1381 REFERENCES [1] Tiwari M, Ranabhat S, Maharjan S. Clinico-histopathological correlation of leprosy: A retrospective study of skin biopsy specimens in Chitwan Medical College. International Journal of Medical Science Research and Practice 2015; 2(1):8-11. [2] Park JE, Park K. Epidemiology of communicable diseases. In: Preventive and Social Medicine. Jabalpur: Banarasidas Bhanol; 1991. p. 215-25. [3] Sharma A, Kumar RS, Goswsami CK, Bardwaj S. Clinicohistopathological correlation in leprosy. JK Sci 2008; 10:120-3. [4] Manandhar U, Adhikari RC, Sayami G. Clinico-histopathological correlation of skin biopsies in leprosy. J Pathol Nepal 2013; 3:452-8. [5] Murthy M. Suryanarayana, Gitu Duara, K. Kasi Viswanath, Kiran Kanth. Clinical and Histopathological Correlation in Hansen’s Disease. Journal of Evolution of Medical and Dental Sciences 2015; 4(35): 6081-6085. [6] Mathur MC, Ghimire RBK, Shrestha P, Kedia SK. Clinicohistopathological Correlation in Leprosy. Kathmandu Univ Med J. 2011; 36(4):248-51. [7] Giridhar M, Arora G, Lajpal K, Chahal KS. Clinicohistopathological concordance in Leprosy- A Clinical, Histopathological and Bacteriological study of 100 cases. Indian J Lepr 2012; 84:217-25. [8] Mistry A S, Rathod S P, Agarwal P. An institution-based observational study to identify sensitive histopathological parameters in leprosy. 2015; 4(12):1720-25 [9] Chauhari B, Mehta RP. Clinico-histopathological correlation in Leprosy. International Journal of Scientific Research, 2012;1(5): 104-105. International Journal of Life Sciences Scientific Research (IJLSSR) Open Access Policy Authors/Contributors are responsible for originality, contents, correct references, and ethical issues. IJLSSR publishes all articles under Creative Commons Attribution- Non-Commercial 4.0 International License (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/legalcode How to cite this article: Anusha KS, Prabhu MH, Dombale VD: Study of Histomorphological Spectrum of Lesions in Leprosy- One Year Study in S N Medical College, Bagalkote. Int. J. Life. Sci. Scienti. Res., 2017; 3(5):1377-1381. DOI:10.21276/ijlssr.2017.3.5.19 Source of Financial Support: Nil, Conflict of interest: Nil