Trichotillomania: a good response to treatment with N-acetylcysteine.

Trichotillomania is considered a behavioral disorder and is characterized by the recurring habit of pulling one's hair, resulting in secondary alopecia. It affects 1% of the adult population, and 2 to 4.4% of psychiatric patients meet the diagnostic criteria. It can occur at any age and is more prevalent in adolescents and females. Its occurrence in childhood is not uncommon and tends to have a more favorable clinical course. The scalp, eyebrows and eyelashes are the most commonly affected sites. Glutamate modulating agents, such as N-acetylcysteine, have been shown to be a promising treatment. N-acetylcysteine acts by reducing oxidative stress and normalizing glutaminergic transmission. In this paper, we report a case of trichotillomania with an excellent response to N-acetylcysteine.

Trichotillomania: a good response to treatment with N-acetylcysteine

Abstract: Trichotillomania is considered a behavioral disorder and is characterized by the recurring habit of pulling one's hair, resulting in secondary alopecia. It affects 1% of the adult population, and 2 to 4.4% of psychiatric patients meet the diagnostic criteria. It can occur at any age and is more prevalent in adolescents and females. Its occurrence in childhood is not uncommon and tends to have a more favorable clinical course. The scalp, eyebrows and eyelashes are the most commonly affected sites. Glutamate modulating agents, such as N-acetylcysteine, have been shown to be a promising treatment. N-acetylcysteine acts by reducing oxidative stress and normalizing glutaminergic transmission. In this paper, we report a case of trichotillomania with an excellent response to N-acetylcysteine.

Hanseníase virchowiana pruriginosa em idoso: a importância do exame dermatoneurológico e suspeição diagnóstica / Itching lepromatous leprosy in an elderly man: the importance of dermatologic and neurological examination and the diagnosis' suspicion

INTRODUÇÃO: A hanseníase virchowiana (MHV) polar é forma clínica de diagnóstico mais difícil nas fases iniciais, já que o comprometimento neurológico é tardio e não há presença de placas. Relata-se um caso com sintoma atípico em idoso: o prurido. RELATO DE CASO: Homem, 81 anos, branco, procedente de Itirapina - SP, encaminhado ao serviço de referência com hipótese diagnóstica de "alergia", relatava que há dois anos notou a presença de pápulas, placas e nódulos em corpo, associado a prurido intenso generalizado, mais pronunciado nas lesões. Ao exame físico, havia livedo reticular difuso que poupava a área do polígono de Michaelis, acrocianose, madarose, pápulas, placas e nódulos eritêmato-violáceos em abdome, região perimamilar, membros inferiores e região glútea. Ao exame neurológico, notou-se espessamento de nervos ulnares, radiais, tibiais e fibular esquerdo. Não apresentava garra ulnar e o teste de sensibilidade com monofilamentos não demonstrou perda da sensibilidade tátil nas mãos ou protetora nos pés. A baciloscopia de pontos índices variou entre de 3 a 5+, com índice morfológico de 3%. O teste de Mitsuda foi negativo, e a biópsia de uma das lesões evidenciou MHV. DISCUSSÃO: A MHV polar constitui-se na forma mais bacilífera e de maior dificuldade diagnóstica, quando não se faz a suspeição. A virtual ausência de imunidade permite que o bacilo prolifere na célula nervosa por quase uma década, em média, sem que haja sintomas característicos (nódulos, "manchas", neurite ou deformidades). Embora seja sintoma atípico, a xerose cutâneo-mucosa pode causar prurido, e o comprometimento neurovascular leva ao livedo reticular e acrocianose, sinais que devem alertar o clínico para a suspeita diagnóstica,...

INTRODUCTION: Polar lepromatous leprosy (LLp) is a clinical form which the diagnosis is very difficult in early stages, since nerve damage is not seen, and there are not visible plaques. We report a case with atypical symptoms in an elderly man: the pruritus.CASE REPORT: Male, 81 years, caucasian, coming from Itirapina - SP, referred to the dermatological service with the diagnosis of "allergy", reported that two years ago noted the presence of papules, plaques and nodules on the body, associated with intense pruritus, more pronounced on the lesions. Physical examination revealed diffuse livedo (which was not seen only on the area of the Michaelis polygon), as weel as acrocyanosis, madarosis, papules, plaques, and erythematous-violaceous nodules on the abdomen, perimamilar region, legs and buttocks. On neurological examination it was noted nerves thickening: both ulnars, radials, tibials, and left fibular. He had no ulnar claw and sensitivity test monofilaments showed no loss of tactile sensitivity on the hands, or even loss of protective sensitivity on the feet. Bacilloscopy of smear from index points ranged from 3-5+, with morphological index = 3%. The Mitsuda test was negative, and biopsy of the lesions showed LL.DISCUSSION: The LLp is the most infectious form of leprosy, and it is the most difficult to make diagnosis, mainly when do not suspected. The virtual lack of immunity allows the bacilli proliferate in the nerve cell for nearly a decade, on average, without typical symptoms (lumps, "stains", neuritis or deformities). Although atypical symptom, mucocutaneous xerosis can cause itching, and neurovascular involvement leads to livedo reticularis and acrocyanosis, signs that should alert the clinician to the diagnosis,...