Histoid Leprosy in an HIV Positive Patient Taking Cart

Total Page:16

File Type:pdf, Size:1020Kb

Histoid Leprosy in an HIV Positive Patient Taking Cart Lepr Rev (2010) 81, 221–223 CASE REPORT Histoid leprosy in an HIV positive patient taking cART R. A. BUMB, B. C. GHIYA, R. JAKHAR & N. PRASAD Department of Dermatology, Venereology and Leprosy, S P Medical College, Bikaner, Rajasthan, India Accepted for publication 09 July 2010 It is well known that HIV infected patients are more susceptible to infection with M. tuberculosis, but this is not clear for M. leprae. Only a few studies have reported this coexistence. Co-infected cases have been reported in the past in the whole spectrum of leprosy i.e. tuberculoid,1 borderline,2 and lepromatous.3,4 The deficiency of cell mediated immunity in leprosy is specific to M. leprae antigen and probably, the reason why the clinical course of leprosy is not influenced by HIV infection.5 When HIV positive patients are treated with highly active anti-retroviral treatment (cART) there is treatment-induced recovery of the immune system of the host which may lead to immune reconstitution inflammatory syndrome (IRIS). Various authors have reported tuberculoid leprosy6,7 and Type I lepra reaction8 as a manifestation of IRIS in HIV positive patients. We are reporting an HIV positive patient who developed histoid leprosy in spite of taking cART for 9 months, without any signs and symptoms of IRIS. Case report: A 42 year old married, male truck driver, presented with genital ulcers to the Department of Dermatology, SP Medical College, Bikaner. He gave a history of multiple unprotected acts of sexual intercourse with many roadside prostitutes in different parts of the country for many years. On examination, there were superficial serpigenous painless ulcers over the glans and prepuce. Clinically he was diagnosed as a case of herpes genitalis and treated with oral and topical acyclovir. A history of high-risk behaviour prompted an HIV test, which was performed after pre-test counselling, and found to be reactive by Tridot as well as ELISA test. The VDRL test was non-reactive. IgG and IgM antibodies against HSV-2 were raised. He refused tests for CD4 þ cell count, viral load and cART due to financial constrains. Post test counselling was then done. After 2 months the patient returned with herpes genitalis along with oral candidiasis. He was treated with oral acyclovir and fluconazole. Routine haematological investigations were within normal limits except raised ESR. CD4 þ cell count was 150/mm3 and viral load of HIV was 1, 55 000 copies/mL. He was counselled and cART was started with a combination of zidovudine, lamivudine and nevirapine, which was well tolerated. After 9 months of cART therapy he returned with generalised skin coloration, shiny, non-itchy, painless and non-tender, discrete, Correspondence to: R.A. Bumb, H-3, PBM Hospital Campus, Bikaner -334001, Rajasthan, INDIA (Tel: þ91 151 2226322; e-mail: [email protected]) 0305-7518/10/064053+03 $1.00 q Lepra 221 222 R. A. Bumb et al. Figure 1. Papulo-nodular lesions of histoid leprosy over the back in an HIV positive patient. papulo-nodular lesions distributed symmetrically all over the body including oral mucous membrane and tongue which had been present for the last one and half months (Figures 1 and 2). The lesions were not associated with fever, joint pains and lymphadenopathy. The peripheral nerves were not thickened, and there was no glove or stocking anaesthesia. Systemic examination was normal. VDRL and TPHA tests were again non-reactive. An X-ray on his chest was normal, and PCR for Mycobacterium avium intracellulare was negative in a skin biopsy specimen. The CD4 þ cell count was 400 cells/mm.3 The slit skin smear from a nodule was highly positive for Mycobacterium leprae, and the histopathological findings were consistent with Histoid leprosy (Figure 3). MB-MDT was started along with cART, and Efavirenz was substituted for Nevirapine. The lesions had completely regressed after a year, but MDT was continued for 1 more year. The patient was lost to follow up after 2 years. Figure 2. Nodules of histoid leprosy over the tongue in an HIV positive patient. Histoid leprosy in an HIV positive patient 223 Figure 3. Biopsy showing the spindle shaped cell characteristics of histoid leprosy (hematoxylin and eosin £ 10). Leprosy in HIV infected patients have been reported, and most of them were either in untreated HIV positive patients,1–4 or as a manifestation of IRIS,6–8 while this patient developed histoid leprosy during anti-retroviral treatment without showing any signs and symptoms of IRIS. In our case neither HIV infection nor cART influenced the course of leprosy, as the patient developed histoid leprosy in spite of taking cART for 9 months. This observation is consistent with the study by Jacob et al.5 who reported that the clinical course of leprosy is not influenced by HIV infection. In the present case even after increase in CD4 þ counts from 150 to 400 cells/mm,3 the patient developed histoid leprosy rather than reversal reaction, which may reflect the poor specific host immune response to M. leprae in HIV co-infection. We excluded Mycobacterium avium intracellulare infection which may mimic histoid leprosy by PCR in skin biopsy spcimens.9 Ethical approval was not required for this study. References 1 Goodle DR, Viciana AL, Pardo RJ et al. Borderline tuberculoid Hansen’s disease in AIDS. J Am Acad Dermatol, 1994; 30: 866–869. 2 Rath N, Kar HK. Leprosy in HIV infection: report of three cases. Ind J Lepr, 2003; 75: 355–359. 3 Gupta TSC, Sinha PK, Murthy VS, Kumari GS. Leprosy in an HIV infected person. J Sex Trans Dis, 2007; 28: 100–102. 4 Borgdoff MW, Van Den Broek J, Chum HJ et al. HIV infection as a risk factor for leprosy: a case control study in Tanzania. Int J Lepr Other Mycobact Dis, 1993; 61: 556–561. 5 Jacob M, George S, Pulimood S et al. Short-term follow-up of patients with multibacillary leprosy and HIV infection. Int J Lepr Other Mycobact Dis, 1996; 64: 392–395. 6 Lawn SD, Wood C, Lockwood DN. Borderline tuberculoid leprosy: an immune reconstitution phenomenon in a human immunodeficiency virus infected person. Clin Infect Dis, 2003; 36: 5–6. 7 Couppie P, Abel S, Voinchet H et al. Immune reconstitution inflammatory syndrome associated with HIV and leprosy. Arch Dermatol, 2004; 140: 997–1000. 8 Kharkar V, Bhor UH, Mahajan S, Khopkar U. Type 1 lepra reaction presenting as immune reconstitution inflammatory syndrome. Indian J Dermatol Venereol Leprol, 2007; 73: 253–256. 9 Boyd AS, Robbins J. Cutaneous mycobacterium avium intracellulare infection in a HIVþ patient mimicking histoid leprosy. Am J Dermatopthol, 2007; 29: 422..
Recommended publications
  • (ERYTHEMA NODOSUM LEPROSUM) the Term
    ? THE HISTOPATHOLOGY OF ACUTE PANNICULITIS NODOSA LEPROSA (ERYTHEMA NODOSUM LEPROSUM) w. J. PEPLER, M.B., Ch.B. Department of Pathology, South African Institute for Medical Research, Johannesburg R. KOOIJ, M.D. Westfort Institution, Pretoria AND J. MARSHALL, M.D. University of Pretoria, Pretoria The term "erythema nodosum leprosum" has frequently appeared in the literature on leprosy since the 1930's, apparently popularized by the Japanese (9). The occurrence of "erythema nodosum" in leprosy had previously been noted at the end of the nineteenth century by Brocq (6) and by Hansen and Looft (8), but the term seems to have fallen into disuse. As will become clear from our clinical and histological descriptions of the phenomenon commonly known as erythema nodosum leprosum, we believe the title to be a misnomer. We suggest that it would be more accurate to call it panniculitis nodosa leprosa (P.N.L,). This condition is commonly confused with acute lepra reaction, both processes being referred to as "acute reactions"; but a sharp line of distinction must be drawn between them. P.N.L. occurs only in patients with lepromatous leprosy as an acute, subacute or chronic skin eruption, with or without fever. It is characterized by showers of dusky red nodules, 0.5 to 2 cm. in diameter, on the extensor surfaces of the limbs, on the face, and, less often, on the trunk. The number of lesions appearing in an attack varies from a few to several hundreds, and they sometimes coalesce to form plaques. The nodules may be painful, and they are usually tender to touch.
    [Show full text]
  • Chapter 3 Bacterial and Viral Infections
    GBB03 10/4/06 12:20 PM Page 19 Chapter 3 Bacterial and viral infections A mighty creature is the germ gain entry into the skin via minor abrasions, or fis- Though smaller than the pachyderm sures between the toes associated with tinea pedis, His customary dwelling place and leg ulcers provide a portal of entry in many Is deep within the human race cases. A frequent predisposing factor is oedema of His childish pride he often pleases the legs, and cellulitis is a common condition in By giving people strange diseases elderly people, who often suffer from leg oedema Do you, my poppet, feel infirm? of cardiac, venous or lymphatic origin. You probably contain a germ The affected area becomes red, hot and swollen (Ogden Nash, The Germ) (Fig. 3.1), and blister formation and areas of skin necrosis may occur. The patient is pyrexial and feels unwell. Rigors may occur and, in elderly Bacterial infections people, a toxic confusional state. In presumed streptococcal cellulitis, penicillin is Streptococcal infection the treatment of choice, initially given as ben- zylpenicillin intravenously. If the leg is affected, Cellulitis bed rest is an important aspect of treatment. Where Cellulitis is a bacterial infection of subcutaneous there is extensive tissue necrosis, surgical debride- tissues that, in immunologically normal individu- ment may be necessary. als, is usually caused by Streptococcus pyogenes. A particularly severe, deep form of cellulitis, in- ‘Erysipelas’ is a term applied to superficial volving fascia and muscles, is known as ‘necrotiz- streptococcal cellulitis that has a well-demarcated ing fasciitis’. This disorder achieved notoriety a few edge.
    [Show full text]
  • A Clinicopathological Analysis of Granulomatous
    JK SCIENCE ORIGINAL ARTICLE A Clinicopathological Analysis of Granulomatous Dermatitis : 4 Year Retrospective Study Jyotsna Suri, Subhash Bhardwaj, Rita Kumari, Shailija Kotwal Abstract The present study was carried out with an attempt to study the incidence of granulomatous dermatitis in hospital based population and to classify and compare the granulomatous dermatitis on the basis of histopathology and find the etiology. This is a four year retrospective study done on the data available in the dermatopathology section of department of pathology. The cases diagnosed as granulomatous dermatitis were retrieved, clinical data and the histopathological features compared to know the incidence of various etiologies of GD. Out of 310 cases of GD with male to female ratio 2.03:1, leprosy comprised major reported etiology (n-244) followed by tuberculosis (n-44), sarcoidosis (n-4), Leshmania Donovani (n-14)) granuloma annulare (n-1) and 3 granulomatous lesions not further classified. Infections form the commonest form of GD out of which leprosy forms the major group. Role of histopathology(H&E and special stains) is very important in confirming the diagnosis of granulomatous dermatitis . Key Words Granuloma, Dermatitis, Inflammatory, Tissue Injury Introduction Granuloma is defined as a focal chronic inflammatory dermatitis presents a diagnostic challenge, many a times. response to tissue injury, characterised by focal, compact The granulomatous dermatitis comprise a large family collection of inflammatory cells, principally of the activated sharing the common histological denominator of histiocytes, modified epitheloid macrophages & granulomas formation. Rightly said that in granulomatous multinucleate giant cells that may or may not be rimmed dermatitis, an identical histologic picture may be produced by lymphocytes and show central necrosis.
    [Show full text]
  • 6/12/2018 1 Infectious Dermatopathology
    6/12/2018 Infectious Dermatopathology – What is “bugging” you? Alina G. Bridges, D.O. Associate Professor Program Director, Dermatopathology Fellowship ASDP Alternate Advisor to the AMA-RUC Department of Dermatology, Division of Dermatopathology and Cutaneous Immunopathology Mayo Clinic, Rochester Disclosures ▪Relevant Financial Relationships ▪None ▪Off Label Usage ▪No Background ▪ One of the most challenging tasks in medicine is the accurate and timely diagnosis of infectious diseases ▪ Classically, infectious disease diagnosis is under the domain of the microbiology laboratory ▪ Culture ▪ May not be performed due to lack of clinical suspicion ▪ Time consuming ▪ Not possible for some organisms ▪ May fail to grow organism due to prior antibiotic treatment, sampling error 1 6/12/2018 Background, continued ▪ Infectious diseases has always played a significant role in our specialty ▪ Many infectious diseases have primary skin manifestations ▪ Dermatopathologists offer invaluable information: ▪ Knowledge of inflammatory patterns and other similar appearing non-infectious conditions ▪ Visualize microorganisms and associated cellular background ▪ Colonization versus Invasion Course Objectives At the end of this course, participants should be able to: ▪ Identify common and important infectious organisms in dermatopathology specimens based on histopathologic features ▪ Develop an appropriate differential diagnosis based on morphologic features, clinical presentation, exposure history, and corresponding microbiology results ▪ Use an algorithm
    [Show full text]
  • INTERNATIONAL JOURNAL of LEPROSY Volume 72, Number 1 Printed in the U.S.A
    INTERNATIONAL JOURNAL OF LEPROSY Volume 72, Number 1 Printed in the U.S.A. (ISSN 0148-916X) INTERNATIONAL JOURNAL OF LEPROSY and Other Mycobacterial Diseases VOLUME 72, NUMBER 1MARCH 2004 Relapses in Multibacillary Patients Treated with Multi-drug Therapy until Smear Negativity: Findings after Twenty Years1 Gift Norman, Geetha Joseph, and Joseph Richard2 ABSTRACT The Schieffelin Leprosy Research and Training Center at Karigiri, India participated in several of the World Health Organization (WHO) trials. The first trial on combined therapy in multi-bacillary leprosy was initiated in 1981. The main objectives of this field trial were to evaluate the efficacy of WHO recommended regimens in preventing relapses, especially drug resistance relapses. This paper reports on the relapses twenty years after patients were inducted into the WHO field trial. Between 1981 and 1982, 1067 borderline lepromatous and lepromatous patients were in- ducted into the WHO field trial for combined therapy in multi-bacillary leprosy trial. Among them, 357 patients were skin smear positive. During the follow-up in 2002, only 173 of them could be traced and assessed. The mean duration of follow-up was 16.4 ± 1.83 years. Two patients relapsed 14 and 15 years after being released from treatment, the relapse rate being 0.07 per 100 person years follow-up. Drug susceptibility tests done on one of the relapsed patients revealed drug sensitive organisms to all multi-drug therapy drugs. RÉSUMÉ Le centre de recherche et de formation de Schieffelin à Karigiri aux Indes a participé à plusieurs études cliniques sponsorisées par l’Organisation Mondiale de la Santé (OMS).
    [Show full text]
  • Wade Histoid Leprosy: Histological and Immunohistochemical Analysis
    Lepr Rev (2013) 84, 176–185 Wade histoid Leprosy: histological and immunohistochemical analysis DANIELA A.M. DA COSTA*, MI´LVIA M.S.S. ENOKIHARA**, SUELY NONOGAKI***, SOLANGE M. MAEDA****, ADRIANA M. PORRO**** & JANE TOMIMORI**** *Medical resident, Escola Paulista de Medicina/UNIFESP, Sa˜o Paulo, Brazil **Department of Pathology, Escola Paulista de Medicina/UNIFESP, Sa˜o Paulo, Brazil ***Pathology Center, Instituto Adolfo Lutz, Sa˜o Paulo, Brazil ****Department of Dermatology, Escola Paulista de Medicina/UNIFESP, Brazil Accepted for publication 1 October 2013 Summary Histoid leprosy is a rare multibacillary form that presents with disseminated papule-nodular cutaneous lesions. To study the inflammatory infiltrate of the histoid form and to compare it with other lepromatous forms, we performed histological and immunohistochemical analysis on skin biopsies. Fifteen patients were included for histopathological analysis (10 histoid and five lepromatous) via the haematoxylin-eosin and Ziehl-Neelsen-Faraco stains. Thus, immunohistochemical techniques using immunoperoxidase assay were performed for: anti-BCG, anti-M. leprae, anti-CD8, anti-CD3, anti-CD20, anti-S100, anti-CD1a, anti-CD68 and anti- vimentin. Spindle cells were present in all histoid patients. A pseudocapsule was observed in half of both studied forms. A comparison using the Ziehl-Neelsen-Faraco stain to evaluate anti-BCG and anti-M.leprae showed no major differences. The CD3þ cells were more pronounced in the histoid form than the lepromatous form. There was greater immunoreactivity toward CD8þ cells in the histoid form, as well as the CD20þ cell count. A similar count of S100þ cells in the epidermis of both leprosy forms was observed. There was a slight increase of dendritic cells in the histoid patients in the superficial and deep dermis.
    [Show full text]
  • 2016 Essentials of Dermatopathology Slide Library Handout Book
    2016 Essentials of Dermatopathology Slide Library Handout Book April 8-10, 2016 JW Marriott Houston Downtown Houston, TX USA CASE #01 -- SLIDE #01 Diagnosis: Nodular fasciitis Case Summary: 12 year old male with a rapidly growing temple mass. Present for 4 weeks. Nodular fasciitis is a self-limited pseudosarcomatous proliferation that may cause clinical alarm due to its rapid growth. It is most common in young adults but occurs across a wide age range. This lesion is typically 3-5 cm and composed of bland fibroblasts and myofibroblasts without significant cytologic atypia arranged in a loose storiform pattern with areas of extravasated red blood cells. Mitoses may be numerous, but atypical mitotic figures are absent. Nodular fasciitis is a benign process, and recurrence is very rare (1%). Recent work has shown that the MYH9-USP6 gene fusion is present in approximately 90% of cases, and molecular techniques to show USP6 gene rearrangement may be a helpful ancillary tool in difficult cases or on small biopsy samples. Weiss SW, Goldblum JR. Enzinger and Weiss’s Soft Tissue Tumors, 5th edition. Mosby Elsevier. 2008. Erickson-Johnson MR, Chou MM, Evers BR, Roth CW, Seys AR, Jin L, Ye Y, Lau AW, Wang X, Oliveira AM. Nodular fasciitis: a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. Lab Invest. 2011 Oct;91(10):1427-33. Amary MF, Ye H, Berisha F, Tirabosco R, Presneau N, Flanagan AM. Detection of USP6 gene rearrangement in nodular fasciitis: an important diagnostic tool. Virchows Arch. 2013 Jul;463(1):97-8. CONTRIBUTED BY KAREN FRITCHIE, MD 1 CASE #02 -- SLIDE #02 Diagnosis: Cellular fibrous histiocytoma Case Summary: 12 year old female with wrist mass.
    [Show full text]
  • Histopathological Study of Granulomatous Dermatoses - a 2 Year Study at a Tertiary Hospital
    International Journal of Health Sciences and Research www.ijhsr.org ISSN: 2249-9571 Original Research Article Histopathological Study of Granulomatous Dermatoses - A 2 Year Study at a Tertiary Hospital Velpula Nagesh Kumar1*, Kotta. Devender Reddy2**, N Ezhil Arasi3** 1Tutor, 2Associate Professor, 3Professor & Head, *Department of Pathology, Rajiv Gandhi Institute of Medical Sciences (RIMS), Govt. Medical Collage, Kadapa, Andhra Pradesh. **Department of Pathology, Osmania Medical Collage, Hyderabad, Telangana. Corresponding Author: Velpula Nagesh Kumar Received: 14/07/2016 Revised: 10/08/2016 Accepted: 11/08/2016 ABSTRACT Granulomatous inflammation is a type of chronic inflammation that has distinctive pattern of presentation with wide etiology and can involve any organ. Pathologists come across this lesion frequently and through knowledge of granulomatous lesions are very much essential to discriminate them from other lesions in the skin as they closely mimic each other. The aim of the present study is know the types of dermal granulomas, their prevalence, age and sex distribution, modes of presentation and histopathological spectrum. This prospective study was undertaken at Osmania General Hospital, Hyderabad from June 2012 to May 2014. A total of 620 skin biopsies were received at the Department of Pathology, histopathological sections of all the cases were critically analyzed and were classified on a “pattern based” approach according to Rabinowitz and Zaim et al. 172 cases were categorized histopathologically as granulomatous dermatoses. Granulomatous dermatoses were more common in males and the peak age of incidence was in 3rd decade. Incidence of Granulomatous dermatoses was 27.7% which was comparable with available literature. In the present study we found that Infections form an important cause of granulomatous dermatoses with majority of cases being leprosy followed by cutaneous tuberculosis and foreign body granulomas.
    [Show full text]
  • UC Davis Dermatology Online Journal
    UC Davis Dermatology Online Journal Title Wade histoid leprosy revisited Permalink https://escholarship.org/uc/item/5d78t619 Journal Dermatology Online Journal, 22(2) Authors Coelho de Sousa, Virginia Laureano, Andre Cardoso, Jorge Publication Date 2016 DOI 10.5070/D3222030092 License https://creativecommons.org/licenses/by-nc-nd/4.0/ 4.0 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Volume 22 Number 1 February 2016 Case presentation Wade histoid leprosy revisited Virgínia Coelho de Sousa, André Laureano, Jorge Cardoso Dermatology Online Journal 22 (2): 8 Department of Dermatology and Venereology, Hospital de Santo António dos Capuchos – Centro Hospitalar de Lisboa Central, Lisboa, Portugal Correspondence: Virgínia Coelho de Sousa, MD Hospital de Santo António dos Capuchos – Centro Hospitalar de Lisboa Central, Lisboa, Portugal Alameda Santo António dos Capuchos, 1169-050 Lisboa, Portugal [email protected] +351926826029 Abstract An 18-year-old man presented with a 4-year history of erythematous patches on the trunk, followed 2-years later by multiple nodules, mostly located on the limbs, and distal paresthesias. Two close contacts were treated for leprosy during his childhood. Histopathological examination revealed a histiocytic infiltrate with acid-fast bacilli on Ziehl-Neelsen stain. The slit-skin and nasal smears showed numerous acid-fast bacilli. The correlation between clinical, epidemiological, histopathological, and microbiological features allowed the diagnosis of lepromatous leprosy, histoid variant. Multidrug therapy as recommended by the WHO was initiated. A rapid and sustained improvement was seen. Histoid leprosy is a rare manifestation of lepromatous leprosy, first described by Wade in 1960. Since then few cases have been reported, the majority of them from countries with a high prevalence of the disease.
    [Show full text]
  • Leprosy in Refugees and Migrants in Italy and a Literature Review of Cases Reported in Europe Between 2009 and 2018
    microorganisms Article Leprosy in Refugees and Migrants in Italy and a Literature Review of Cases Reported in Europe between 2009 and 2018 Anna Beltrame 1,* , Gianfranco Barabino 2, Yiran Wei 2, Andrea Clapasson 2, Pierantonio Orza 1, Francesca Perandin 1 , Chiara Piubelli 1 , Geraldo Badona Monteiro 1, Silvia Stefania Longoni 1, Paola Rodari 1 , Silvia Duranti 1, Ronaldo Silva 1 , Veronica Andrea Fittipaldo 3 and Zeno Bisoffi 1,4 1 Department of Infectious, Tropical Diseases and Microbiology, I.R.C.C.S. Sacro Cuore Don Calabria Hospital, Via Sempreboni 5, 37024 Negrar di Valpolicella, Italy; [email protected] (P.O.); [email protected] (F.P.); [email protected] (C.P.); [email protected] (G.B.M.); [email protected] (S.S.L.); [email protected] (P.R.); [email protected] (S.D.); [email protected] (R.S.); zeno.bisoffi@sacrocuore.it (Z.B.) 2 Dermatological Clinic, National Reference Center for Hansen’s Disease, Ospedale Policlinico San Martino, Sistema Sanitario Regione Liguria, Istituto di Ricovero e Cura a Carattere Scientifico per l’Oncologia, Largo Rosanna Benzi 10, 16132 Genoa, Italy; [email protected] (G.B.); [email protected] (Y.W.); [email protected] (A.C.) 3 Oncology Department, Mario Negri Institute for Pharmacological Research I.R.C.C.S., Via Giuseppe La Masa 19, 20156 Milano, Italy; vafi[email protected] 4 Department of Diagnostic and Public Health, University of Verona, P.le L. A. Scuro 10, 37134 Verona, Italy * Correspondence: [email protected]; Tel.: +39-045-601-4748 Received: 30 June 2020; Accepted: 23 July 2020; Published: 24 July 2020 Abstract: Leprosy is a chronic neglected infectious disease that affects over 200,000 people each year and causes disabilities in more than four million people in Asia, Africa, and Latin America.
    [Show full text]
  • Leprosy Revisited
    Clinical Dermatology: Research and Therapy Open Access Letter to the Editor Leprosy Revisited Virendra N Sehgal* Dermato-Venereology (Skin/VD) Center, Sehgal Nursing Home, India A R T I C L E I N F O Letter to the Editor Article history: Leprosy [1] is a chronic granlomatous disease involves skin peripheral nerves, Received: 26 June 2018 Accepted: 28 June 2018 nasal mucosa affecting tissues and organs. Demonstration of Causative Published: 30 June 2018 Organism through Slit -Skin smear Examination [2] Mycobacterium leprae / M. Copyright: © 2018 Sehgal VN, Clin Dermatol Res Ther leprae (Figure 1) Ziehl-Neelsen stain Acid fast bacilli. Narrative of M. leprae This is an open access article distributed under the Creative Commons Attribution including its characteristics, mode of transmission pathogenesis, and evolution License, which permits unrestricted use, distribution, and reproduction in any of classification are salient pre-requisite to comprehend leprosy and gender. medium, provided the original work is Mycobacterium leprae: characteristics properly cited. • Appear as straight or curved rods Citation this article: Sehgal VN. Leprosy Revisited. Clin Dermatol Res Ther. 2018; • Size is 1-8 microns x 0.5 microns. 2(1):118. • Polar bodies present as clubbed forms. • Lateral buds • Acid fast but less resistant only 5% H2So4 • Live bacilli, solid uniform structure. • Dead appear as fragmented with granules. Investigations for M. Leprae Bacteriological examination Slit-Skin smears: Made by slit and scrape method from the most active looking edge of skin lesion and stained with Ziehl-Neelsen method. Reading of smears: • Bacteriological-index (BI) Indicates density of leprosy bacilli (live & dead) in the smears and range from 0 to 6+ • Morphological-index (MI) It is the percentage of presumably living bacilli in relation to total number of bacilli in the smear.
    [Show full text]
  • Histoid Leprosy with Giant Lesions of Fingers and Toes
    Biomédica 2015;35:165-70 Lepra histioide doi: http://dx.doi.org/10.7705/biomedica.v35i2.2562 PRESENTACIÓN DE CASO Histoid leprosy with giant lesions of fingers and toes Gerzaín Rodriguez1, Rafael Henríquez2, Shirley Gallo2, César Panqueva2 1 Facultad de Medicina, Universidad de La Sabana, Chía, Colombia 2 Facultad de Medicina, Universidad Surcolombiana, Neiva, Colombia This work was conducted at the Facultad de Medicina, Universidad de La Sabana, and at the Facultad de Medicina, Universidad Surcolombiana. Histoid leprosy, a clinical and histological variant of multibacillary leprosy, may offer a challenging diagnosis even for experts. An 83-year-old woman presented with papular, nodular and tumor-like lesions of 3 years of evolution, affecting fingers, toes, hands, thighs and knees, and wide superficial ulcers in her lower calves. Cutaneous lymphoma was suspected. A biopsy of a nodule of the knee showed a diffuse dermal infiltrate with microvacuolated histiocytes, moderate numbers of lymphocytes and plasma cells. Cutaneous lymphoma was suggested. Immunohistochemistry (IHC) showed prominent CD68-positive macrophages, as well as CD3, CD8 and CD20 positive cells. Additional sections suggested cutaneous leishmaniasis. New biopsies were sent with the clinical diagnoses of cutaneous lymphoma, Kaposi´s sarcoma or lepromatous leprosy, as the patient had madarosis. These biopsies showed atrophic epidermis, a thin Grenz zone and diffuse inflammation with fusiform cells and pale vacuolated macrophages. Ziehl- Neelsen stain showed abundant solid phagocytized bacilli with no globii formation. Abundant bacilli were demonstrated in the first biopsy. Histoid leprosy was diagnosed. The patient received the WHO multidrug therapy with excellent results. We concluded that Ziehl Neelsen staining should be used in the presence of a diffuse dermal infiltrate with fusiform and vacuolated histiocytes, which suggests a tumor, and an IHC particularly rich in CD68-positive macrophages; this will reveal abundant bacilli if the lesion is leprosy.
    [Show full text]