Self-medication in health students from two Brazilian universities

Introduction: Self medication is a component of self care and it is considered as primary public health resource in health care system. It can be defined as use of non-prescription medicines by people on their own initiative. Dentists, together with doctors and veterinarians, comprise the professional classes that may and must prescribe medications for their patients. On the other hand, the nursing professionals are the ones who more administer drugs to patients in the ambulatory and hospital. Objective: This study was aimed to find out the frequency of self medication in selected university students, to find out the difference in the proportions of self medication between dentistry and nursing students, as well to evaluate the students' knowledge of harmful effects of self medication and common problems of students that use the self medication. Material and methods: We were applied 209 questionnaires among dentistry students from the 3rd to 8th semesters at the Paulista University/Goiânia and 542 among nursing students from the 3rd to 8th semesters at the Estacio de Sa University of Goiás. Results and conclusion: In the present study was observed a high rate of self-medication among undergraduate students in the health area, particularly among the dentistry and nurse students. The result was alarming because the professional him/herself who should educate patients and dissuade them from this practice is a habitual user; it makes it more difficult to aspire to the future inhibition and reduction of this practice that is so harmful to health.

Chronic graft versus host disease: a scleroderma-like case report

INTRODUCTION: Chronic graft versus host disease (cGVHD) is the most common consequence of allogeneic bone marrow transplantation, and it is associated with morbidity and mortality. Oral manifestations are diagnosed in approximately 80 percent of patients with chronic GVHD. OBJECTIVE: To present a case of chronic GVHD with scleroderma-like lesions in skin and oral cavity CASE REPORT: A 27-year-old female was admitted, in a Hematology Center, in 1997, with previous diagnosis of chronic myeloid leukemia since 1994. Over past four months after allogeneic BTM she developed cGVHD in eyes, mouth, liver, lungs and skin. The patient presented sclerotic skin changes, hyperkeratosis of hands and xerophthalmia. CONCLUSION: Clinical manifestations of chronic GVHD are similar to autoimmune collagen vascular disease and the two main types of cutaneous chronic GVHD are lichenoid and sclerodermatous.

Atypical appearance of epidermoid cyst in tongue's ventral surface

INTRODUCTION: Epidermoids cysts are benign and rare lesions in oral cavity. It presents as a nodular lesion of sessile base, soft to palpation. In the oral cavity, it most happens on the floor of the mouth's midline. Without treatment, these lesions can lead to dysphagia, dysphonia and dyspnea due to reach a large size. OBJECTIVE: To report a case of a 12-year-old boy presenting a lesion on the tongue's ventral surface causing difficult to swallow. CASE REPORT: The patient was referred to the School of Dentistry of Paulista University, complaining about an asymptomatic nodule on the tongue's ventral surface, lasting for 10 months. Clinical examination showed the extensive fibrous mass on the tongue's medium anterior ventral surface. CONCLUSION: With a clinical diagnosis of dermoid, epidermoid cyst, or lipoma, an excisional biopsy was performed. Histological examination was consistent to the diagnosis of epidermoid cyst. The patient was followed up and 2 years after surgery there was no sign of recurrence.

Synchronous pleomorphic adenoma and periapical cyst: clinical case report / Adenoma pleomorfo e cisto periapical sincrônicos: relato de caso clínico

The pleomorphic adenoma or mixed benign tumor is the most common benign neoplasia of the salivary gland in human beings. It preferentially occurs in the superficial lobe of the parotid gland. In the oral cavity, associated with the minor salivary glands, it has a greater predilection for the palate region, with slight predisposition in women between the 3rd and 4th decades of life. The radicular cyst is an odontogenic inflammatory cyst resulting from pulp lesions caused by traumas or caries. In spite of being relatively common, there are no reports of association with salivary gland tumors. The aim of this work is to report a case of a 36-year-old woman patient, who presented with synchronous development of a pleomorphic adenoma and periapical cyst within the same region. The option taken was to perform enucleation of both lesions,followed by local curettage. The patient has been followed-up clinically and radiographically for around 18 months without signs of recurrence.

O adenoma pleomórfico ou tumor misto benigno é a neoplasia benigna mais comum primária de glândula salivar. Ocorre preferencialmente no lobo superficial da glândula parótida. Na cavidade oral, associado com as glândulas salivares menores, tem uma maior predileção para a região do palato, com ligeira predisposição em mulheres entre a 3 ª e 4 ª décadas de vida. O cisto radicular é um cisto odontogênico inflamatório decorrente de lesões causadas por traumas ou cárie. Apesar de ser relativamente comum, não há relatos de cistos periapicais associados com tumores de glândula salivar. O objetivo deste artigo é relatar um caso de uma paciente de 36 anos de idade com desenvolvimento sincrônico de adenoma pleomorfo e cisto periapical em uma mesma região. A opção tomada foi a de realizar a enucleação de ambas as lesões, seguido de curetagem local. A paciente está sendo acompanhada clínica e radiograficamente por cerca de 18 meses sem sinais de recidiva.

Calcifying cystic odontogenic tumor radiographically mimicking a lateral periodontal cyst: clinical case report / Tumor odontogênico cístico calcificante mimetizando radiograficamente o cisto periodontal lateral: relato de caso clínico

The calcifying cystic odontogenic tumor (CCOT) is a rare odontogenic lesion derived from the remaining odontogenic epithelium of the maxilla or mandible. Its occurrence in the maxilla and mandible is similar, however, the canine region is the most affected when compared with other regions. The aim of this paper is to relate the case of a patient who presented a CCOT in the left region of the maxilla, between the canine and the first premolar, characterized by an increase in volume that was painful on palpation. The lesion presented a well circumscribed radiolucent radiographic image, however, presented no root resorption and radiopacities suggestive of dystrophic calcification, common signs in this tumor. With the diagnostic hypothesis of a lateral periodontal cyst, enucleation of the lesion was performed. The patient has been followed-up for around 15 months without signs of recurrence.

O tumor odontogênico císto calcificante (TOCC) é uma lesão odontogênica rara derivada do epitélio odontogênico remanescente da maxila ou mandíbula. Possui ocorrência semelhante em maxila e mandíbula, porém a região de canino é a mais afetada quando comparada com outras regiões. O objetivo deste estudo é relatar um caso de um paciente que apresenta um TOCC em região esquerda de maxila, entre o canino e o primeiro pré-molar, caracterizado com aumento de volume doloroso à palpação. Radiograficamente a lesão apresentava imagemradiográfica radiolúcida bem circunscrita, no entanto não apresentava reabsorção radicular e radiopacidades sugestivas de calcificação distrófica, sinais comuns neste tumor. Com hipótese diagnóstica de cisto periodontal lateral, foi feita enucleação da lesão. O paciente está em acompanhamento há cerca de 15 meses sem sinais de recorrência.

Sialadenoma papilliferum: case report and review of literature / Sialoadenoma papilífero: relato de caso e revisão da literatura

Sialadenoma papilliferum is a rare tumor benign of the salivary glands, that usually occurs in males older than 50 years. It's frequently found in junction of hard and soft palate, but others sites intraoral mucosa as lips, and parotid gland also can to be affected. A 46 year-old male patient was referred to the University Paulista for dental evaluation and was found a lesion besides of the midline in posterior region in hardpalate. After biopsy had done the histopathology analyze and arrived the diagnosis of sialadenoma papilliferum. The patient was followed at 15 months and none evidence of recurrence was related.

O sialoadenoma papilífero é um tumor benigno raro de glândulas salivares que usualmente ocorre em homens com mais de 50 anos de idade. Normalmente localiza-se na junção do palato mole com o palato duro, entretanto outros locais como lábios, mucosa jugal e glândulas parótidas também podem ser afetados. Paciente de 46 anos de idade, gênero masculino foi encaminhado à Universidade Paulista para avaliação dentária e foi observada uma lesão localizada na linha média em região de palato duro posterior. Após a biópsia e análise histopatológica chegou-se ao diagnóstico de sialoadenoma papilífero. O paciente está em acompanhamento há cerca de 15 meses sem sinais de recorrência.

Cleidocranial dysplasia associated with the dentigerous cyst: review of the literature and report of the clinical case / Displasia cleidocraniana associada a cisto dentígero: revisão da literatura e relato de caso clínico

Cleidocranial dysplasia is a developmental anomaly of the skeleton and teeth. It can be inherited as an autosomal dominant characteristic with high penetrance and variable expressivity. It occurs with equal frequency in both genders and races. The clinical appearance of cleidocranial dysplasia is pathognomonic. The stature is mildly to moderately shortened, with neck appearing long and narrow and the shoulders markedly drooped. Maxillary hypoplasia gives the mandible a relatively prognathic appearance, although some patients may show variable mandibular prognathism due to increased length of the mandible in conjunction with short cranial base. The head and neck features are very variable. Herein, we are described one cleidocranial dysplasia case, in an 84 year female patient, with the dentigerous cyst, which she were not kwon the diagnosis of the her congenital syndrome.

A displasia cleidocraniana é uma alteração de desenvolvimento do esqueleto e dos dentes. É uma desordem autossômica dominante com alta penetrância e expressibilidade variada. Ocorre em igual frequência em ambos os gêneros e raças. Suas características clínicas são patognomônicas. Apresenta estatura baixa a moderada, com aparência do pescoço longo e os ombros caídos. Hipoplasia da maxila gera um aparente prognatismo. As características clinicas em cabeça e pescoço são muito variadas. Este relato descreve um caso de uma paciente de 84 anos com displasia cleidocraniana associada a cisto dentígero a qual não sabia ser portadora de tal síndrome congênita.

Efeitos tardios do transplante de medula óssea alogênico: estudo retrospectivo em 98 pacientes receptores / Late complication of allogeneic bone marrow transplantation: retrospective study of 98 receptor patients / Late complication of allogeneic bone marrow transplantation: retrospective study of 98 receptor patients

Objetivo - A Doença do Enxerto contra o Hospedeiro crônica (DECHc) é uma das mais frequentes complicações tardias do transplante de medula óssea alogênico. A cavidade bucal é o local de maior acometimento desta patologia. Métodos - Este estudo visa investigar a incidência de DECHc, os locais de acometimento, assim como o tipo de lesão em cavidade bucal. Foram avaliados, retrospectivamente, através de prontuários médicos, 98 pacientes que foram submetidos a transplante de medula óssea alogênico no Hemocentro/Unicamp, em um período de um ano. Foram analisadas a presença ou ausência da DECH crônica, os sítios de maior acometimento das lesões e, quando em cavidade bucal, os locais e aspecto clínico mais importantes. Resultados e Conclusões - Dos 98 pacientes, 64 apresentavam DECHc. Destes, 51 apresentavam envolvimento bucal. Em boca, 27 foram em mucosa bucal e a forma clinica mais frequente foi a liquenóide. Nenhum fator encontrado pode contribuir com a severidade da DECHc em cavidade bucal assim como suas manifestações clínicas.

Objective - Chronic graft versus host disease (cGVHD) is the most common late complication of allogeneic bone marrow transplantation. Oral cavity is the most common site of involvement of cGVHD. Methods - This study sought to investigate the incidence of cGVHD, the site of involvement, as well as the kind of oral lesions that resulted. They had been evaluated through medical handbooks, 98 patients who had been submitted the blood marrow alogenic transplant in the Hemocentro/Unicamp, in a period of one year. The presence or absence of the chronic GVHD had been analyzed, the side of the body injuries and, when in oral cavity, the more important places and clinical aspect. Results and Conclusions - Of ninety eight patients, sixty four were cGVHD. Fifty one patients presented oral involvement. On the oral cavity, twenty seven were on buccal mucosa and the clinic features most prevalent was the lichenoid type. No factor that could contribute to the severity of cGVHD oral lesions was found.

Pemphigus vulgaris in a juvenile patient: case report.

Pemphigus vulgaris is a rare cause of oral mucosal ulceration that mainly affects middle-aged adults; the oral lesions of pemphigus are associated with cutaneous manifestations. This article reports a case of oral phemphigus vulgaris in a 17-year-old girl without any cutaneous lesions. After seven months of steroid therapy, the disease was controlled. Early recognition of this disease may prevent delayed diagnosis and incorrect treatment.

Primary oral and perioral amyloidosis associated with multiple myeloma.

Three years after being diagnosed with multiple myeloma, a patient sought treatment for swelling on the floor of the mouth, associated with hardening of the soft tissues on the right perioral region, loss of facial expression, and difficulty opening his mouth. The patient reported improvement following an incisional biopsy for microscopic diagnosis. Eighteen months later, the patient showed no clinical alterations.

Telangectasia hemorrágica hereditária: relato de caso clínico / Hereditary hemorrhagic telangectasia: repórt of case

Telangectasia Hemorrágica Hereditária, também conhecida como síndrome de Rendu-Osler-Weber, é uma alteração caracterizada por uma displasia fibrovascular associada com a presença de telangectasias e malformações arteriovenosas. Acomete preferencialmente a pele, mucosas, pulmão e cérebro. No passado, era considerada uma doença rara, sem grandes conseqüências na vida dos indivíduos afetados. Entretanto, nos dias atuais, é reconhecida como uma entidade não tão incomum, e quando envolve o cérebro e os pulmões, está associada a altas taxas de mortalidade e morbidade destes pacientes. O objetivo deste estudo foi relatar um caso de telangectasia hemorrágica hereditária no qual a suspeita do diagnóstico foi feita pela detecção de telangectasias intrabucais