Abstract:Histoid leprosy, an uncommon variant of lepromatous leprosy, develops usually as relapse in lepromatous patients who are on dapsone monotherapy, but uncommonly arises de novo. This rare form of the disease, with unique clinical and histopathological features, may pose a diagnostic challenge even to astute clinicians. We report the case that occurred de novo in an elderly who presented with small to large lesions all over the body. A fresh focus on histoid leprosy is the primary objective of this paper, especia… Show more
“…These cases act as reservoirs of leprosy and spread the disease even after a very good control program. Additionally, the prevalence of de novo cases is increasing in the era of leprosy elimination, which is also a point of concern for leprologist to research for a genetic mutation in the bacilli causing drug resistance 9 .…”
Histoid leprosy (HL) is a rare variant of lepromatous leprosy with unique clinical, histopathological, and microbiological features. A 32-year-old man from Malawi who immigrated to Johannesburg 1-year-ago, presented with a 4-month history of flesh-colored nodules on the face and trunk and hyperpigmented plaques on the chest and limbs. Skin slit smears confirmed multibacillary leprosy, and skin punch biopsies showed proliferation of spindled cells containing a large number of acid-fast bacilli. The prevalence of de novo HL is increasing in the era of leprosy elimination. HL cases may act as reservoirs and negatively affect the global control of leprosy.
“…These cases act as reservoirs of leprosy and spread the disease even after a very good control program. Additionally, the prevalence of de novo cases is increasing in the era of leprosy elimination, which is also a point of concern for leprologist to research for a genetic mutation in the bacilli causing drug resistance 9 .…”
Histoid leprosy (HL) is a rare variant of lepromatous leprosy with unique clinical, histopathological, and microbiological features. A 32-year-old man from Malawi who immigrated to Johannesburg 1-year-ago, presented with a 4-month history of flesh-colored nodules on the face and trunk and hyperpigmented plaques on the chest and limbs. Skin slit smears confirmed multibacillary leprosy, and skin punch biopsies showed proliferation of spindled cells containing a large number of acid-fast bacilli. The prevalence of de novo HL is increasing in the era of leprosy elimination. HL cases may act as reservoirs and negatively affect the global control of leprosy.
“…In severe cases mucosa and genitalia may also be involved. The sites usually spared are the palms and soles [2]. An excoriated lesion found in our case was due to itching which could be due to increased proliferation of mast cells and their degranulation in the histoid nodule [6].…”
Section: Discussionmentioning
confidence: 99%
“…Bacteriologically, bacilli are longer than the normal, are uniform in length, more often solid with tapering ends and are arranged in parallel bundles along the long axis of the histiocytes (histoid habitus) without globus formation. Histopathologically, fusiform histiocytes are seen arranged in a whorled, criss-cross, or storiform pattern [2,3]. It can occur as relapse following dapsone monotherapy, incomplete therapy, resistance to antileprosy drugs, following multidrug therapy (MDT) and may in rare occasion arise de novo [4] but the exact etiopathogenesis is not clarified yet [5].…”
Histoid leprosy is a rare variant of lepromatous leprosy with unique clinical, immunological, bacteriological & histopathological features. It can occur as relapse following dapsone monotherapy, incomplete therapy, resistance to antileprosy drugs, following MDT & may in rare occassion de-novo. Here, we are presenting a case of histoid leprosy with candidal onychomycosis in middle aged army personnel who had taken incomplete therapy earlier.
Histoid Hansen's disease is a rare form of multibacillary leprosy with distinct clinical and histopathological features. This type of leprosy is a variant of lepromatous leprosy with a very high bacterial reserve. Of alarming concern is the discovery of an isolated mucosal histoid leprotic lesion inside the nasal cavity of a patient in the post-global leprosy elimination era. Our case had no history of leprosy or exposure to dapsone/multidrug therapy but had a heavy bacillary index. We are reporting this case to highlight the rarity of mucosal lesions due to histoid leprosy and involvement of the nasal cavity, as well as to create awareness and avoid misdiagnosis. This will help facilitate prompt treatment to minimize the complications and deformities of the patient and prevent its spread throughout the community.
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