Tuberculides are skin lesions caused by the hematogeneous dissemination of Mycobacterium tuberculosis. Bacilli are rapidly destroyed in the skin and are thus neither visible histologically nor identifiable by culture. Diagnosis depends on previous knowledge of systemic and/or
cutaneous tuberculosis. Lichen scrofulosorum (LS), the most uncommon variant of
tuberculid, is usually associated with M. tuberculosis
infection of lymph nodes or bone but was also reported in association with other mycobacterioses.
OBJECTIVES: In 2008, a 51-year-old woman from the Philippines was diagnosed with
tuberculoid leprosy and treated. In 2010 the
leprosy was considered to have been cured, and treatment was stopped. In 2011 the patient presented with lesions on the trunk and legs. Biopsy specimens were obtained for histopathologic examination and
DNA detection for polymerase chain reaction (PCR).
RESULTS: Histopathology in the biopsy from the trunk revealed the dermis to be diffusely occupied by
granulomas with perineural and periadnexal disposition.
Granulomas were composed of epithelioid cells and lymphocytes. Fite-Faraco staining revealed a few solid
acid-fast bacilli within nerve fascicles.
Reinfection or the re-reactivation of multibacillary
borderline tuberculoid leprosy was diagnosed. Histopathology in the biopsy taken from the leg showed superficial, well-formed
granulomas in the vicinity of hair follicles and sweat ducts. No
acid-fast bacilli were seen. Analysis by PCR revealed M. leprae
DNA in specimens from both the leg and trunk. The clinical features of the papular eruption and the histopathologic findings and concomitant mycobacterial
infection with M. leprae led to a diagnosis of LS. Treatment was commenced with
dapsone 100 mg/day,
clofazimine 50 mg/day and 300 mg/month, and
rifampicin 600 mg/day. The
lichenoid eruption on the legs disappeared at one month of
therapy, whereas the other skin lesions resolved in one year leaving residual hypochromic macules.
CONCLUSIONS: