ABSTRACT
Perforating granuloma annulare (PGA), a rare variant of granuloma annulare, is characterized by transepidermal elimination of altered collagen that clinically manifests an umbilicated papule with a central crust. It can be confused with papulonecrotic tuberculid (PNT) because of their similar appearance. Unlike PGA, PNT is usually related to tuberculosis infection with a typical histologic finding of wedge-shaped dermal necrosis. Here, we report the first Korean case of PGA mimicking PNT both clinically and histologically. A 43-year-old Korean woman presented with erythematous papules localized on the extensor surface of her limbs for one year. Some of these papules had a central umbilication or a crust. Regarding comorbidity, she had latent tuberculosis diagnosed with QuantiFERON®-TB Gold test about five months ago. She was on antituberculous medication. Initially, a diagnosis of papulonecrotic tuberculid accompanied by latent tuberculosis was considered. However, despite taking the antituberculous medication for five months, her skin lesions were not improved. Biopsy specimen from her arm lesion showed wedge-shaped area of necrosis in the dermis. Additionally, there were multiple focal mucin depositions and palisading granulomatous inflammation throughout the dermis. A diagnosis of PGA was made and she was treated with topical corticosteroid. After two weeks of applying topical corticosteroid, most of her skin lesions disappeared, leaving some hyperpigmented scars.
Subject(s)
Adult , Female , Humans , Arm , Biopsy , Cicatrix , Collagen , Comorbidity , Dermis , Diagnosis , Extremities , Granuloma Annulare , Granuloma , Inflammation , Latent Tuberculosis , Mucins , Necrosis , Skin , Tuberculosis , Tuberculosis, CutaneousABSTRACT
Una niña de 12 años fue atendida por presentar pápulas milimétricas diseminadas que involucionaron hacia escaras varioliformes. La prueba de tuberculina fue fuertemente reactiva. Se diagnosticó una tuberculosis pulmonar subyacente y la paciente respondió al tratamiento antituberculoso. La tubercúlide papulonecrótica es una erupción cutánea que se cree debida a hipersensibilidad ante un foco subyacente de tuberculosis y sería un indicador de buen estado inmunitario.
A 12-year-old girl was seen with widespread millimetric papules which resolved leaving varioliform scars. Tuberculin test was strongly reactive. Underlying pulmonary tuberculosis was diagnosed. The patient responded to antituberculous treatment. Papulonecrotic tuberculid is a skin eruption thought to be due to hypersensitivity to an underlying focus of tuberculosis and is an indicator of good immunologic status.
Subject(s)
Child , Female , Humans , Tuberculosis, Cutaneous/pathology , NecrosisABSTRACT
Lymphadenitis is a common manifestation in tuberculous diseases. However, papulonecrotic tuberculid is an uncommon cutaneous manifestation, and is considered an allergic reaction against tuberculous bacilli in tuberculous lesions other than the lymph nodes. A wide great variety of cutaneous manifestations arise over a period of a few weeks - i.e., papules, necrosis, crusted and atrophic scars. We described a 27-year-old woman with right cervical tuberculous lymphadenitis and skin lesions involving her arms, legs and both fingers. Histopathologically, a leukocytoclastic vasculitis with V-shaped epidermal necrosis was observed in the upper and deep dermis, including the good response to anti-tuberculosis therapy support the diagnosis of papulonecrotic tuberculid.
Subject(s)
Adult , Female , Humans , Arm , Cicatrix , Dermis , Diagnosis , Fingers , Hypersensitivity , Leg , Lymph Nodes , Lymphadenitis , Necrosis , Skin , Tuberculosis, Cutaneous , Tuberculosis, Lymph Node , VasculitisABSTRACT
We report a rare case in which two tuberculids, erythema induratum and papulonecrotic tuberculid, occured together. A 15-year-old Korean girl had two types of clinically distinct lesions; painful subcutaneous nodules on the legs and pruritic necrotic papules on the trunk and extremity. Mantoux test showed a strong positive reaction. Histopathologic findings of the subcutaneous nodule and necrotic papule were consistent with erythema induratum and papulonecrotic tuberculid, respectively. There was no extracutaneous focus of tuberculosis. Polymerase chain reaction for tuberculosis bacilli in both lesions revealed negative results. Antituberculous therapy brought a rapid clinical improvement of lesions within a month.
Subject(s)
Adolescent , Female , Humans , Erythema Induratum , Erythema , Extremities , Leg , Polymerase Chain Reaction , Tuberculosis , Tuberculosis, CutaneousABSTRACT
We report an extremely rare case in which two tuberculids, papulonecrotic tuberculid and erythema nodosum, occurred together. A 16-year-old girl had two types of clinically distinct lesions; asymptomatic necrotic papules on the upper and lower extremities and painful subcutaneous nodules on the legs. A Mantoux test showed a strong positive reaction. Histopathologic findings of the necrotic papule and subcutaneous nodule were consistent with papulonecrotic tuberculid and erythema nodosum, respectively. There was no extracutaneous focus of tuberculosis. Polymerase chain reaction for tuberculous bacilli in the papulonecrotic tuberculid lesion revealed a negative result. Antituberculous therapy brought a rapid clinical improvement of both lesions.