TY - JOUR KW - Adult KW - Diagnosis, Differential KW - Humans KW - Leprosy, lepromatous KW - Lymphatic Diseases KW - Male KW - Skin Neoplasms AU - Abdul Razack E M AU - Dharmaraj S AU - Krishnaram A S AU - Selvaraj A M AB -
A 23-year old male presented for evaluation of skin coloured, non-scaly, asymptomatic papulonodules of sizes varying from 0.5 cm to 2 cm of 4 years duration distributed all over the body including the ears. The plaques present on the face gave the appearance of a 'leonine facies'. Clinically mistaken for lepromatous leprosy in reaction the patient was treated with antileprosy and anti-inflammatory drugs in 3 other centres for months with no improvement. Systemic involvement included painful swelling of both knee joints, pericardial effusion episcleritis and enlarged liver. Negative slit smears for AFB from the nodules repeatedly and the histology of one on the skin nodules clinched the diagnosis of multicentric reticulohistiocytosis. The case is reported not only for its rarity, and varying clinical lesions simulating lepromatous leprosy but also to alert the leprologists to avert unreasonable delay in diagnosis.
BT - Indian journal of leprosy C1 - http://www.ncbi.nlm.nih.gov/pubmed/3253341?dopt=Abstract CN - Infolep Library - available DA - 1988 Oct IS - 4 J2 - Indian J Lepr LA - eng N2 -A 23-year old male presented for evaluation of skin coloured, non-scaly, asymptomatic papulonodules of sizes varying from 0.5 cm to 2 cm of 4 years duration distributed all over the body including the ears. The plaques present on the face gave the appearance of a 'leonine facies'. Clinically mistaken for lepromatous leprosy in reaction the patient was treated with antileprosy and anti-inflammatory drugs in 3 other centres for months with no improvement. Systemic involvement included painful swelling of both knee joints, pericardial effusion episcleritis and enlarged liver. Negative slit smears for AFB from the nodules repeatedly and the histology of one on the skin nodules clinched the diagnosis of multicentric reticulohistiocytosis. The case is reported not only for its rarity, and varying clinical lesions simulating lepromatous leprosy but also to alert the leprologists to avert unreasonable delay in diagnosis.
PY - 1988 SP - 604 EP - 8 T2 - Indian journal of leprosy TI - Multicentric reticulohistiocytosis masquerading as lepromatous leprosy. VL - 60 SN - 0254-9395 ER -