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    Eduardo J. S. Honorato
    This document contains summaries of several case reports from dental journals. One case report describes a female patient with systemic lupus erythematosus who presented with an oral ulcerative lesion. Biopsy revealed lichenoid mucositis consistent with SLE involvement of the oral mucosa. Another case report describes a patient with intellectual disabilities who developed a peripheral ossifying fibroma related to the presence of a foreign body. A third case report describes premature loss of both primary and permanent teeth in a child, who was ultimately diagnosed with dentin dysplasia type 1.

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    Eduardo J. S. Honorato
    26 views1 page
    This document contains summaries of several case reports from dental journals. One case report describes a female patient with systemic lupus erythematosus who presented with an oral ulcerative lesion. Biopsy revealed lichenoid mucositis consistent with SLE involvement of the oral mucosa. Another case report describes a patient with intellectual disabilities who developed a peripheral ossifying fibroma related to the presence of a foreign body. A third case report describes premature loss of both primary and permanent teeth in a child, who was ultimately diagnosed with dentin dysplasia type 1.

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    This document contains summaries of several case reports from dental journals. One case report describes a female patient with systemic lupus erythematosus who presented with an oral ulcerative lesion. Biopsy revealed lichenoid mucositis consistent with SLE involvement of the oral mucosa. Another case report describes a patient with intellectual disabilities who developed a peripheral ossifying fibroma related to the presence of a foreign body. A third case report describes premature loss of both primary and permanent teeth in a child, who was ultimately diagnosed with dentin dysplasia type 1.

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    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Download as pdf or txt
    26 views1 page

    04

    Uploaded by

    Eduardo J. S. Honorato
    This document contains summaries of several case reports from dental journals. One case report describes a female patient with systemic lupus erythematosus who presented with an oral ulcerative lesion. Biopsy revealed lichenoid mucositis consistent with SLE involvement of the oral mucosa. Another case report describes a patient with intellectual disabilities who developed a peripheral ossifying fibroma related to the presence of a foreign body. A third case report describes premature loss of both primary and permanent teeth in a child, who was ultimately diagnosed with dentin dysplasia type 1.

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    of 1

    OOOO ABSTRACTS

    Volume 124, Number 2 Abstracts e111

    being SLE the most common type. It affects many organs, ner- associate clinic, radiography and microscopy. Management of
    vous system and can also affect the oral mucosa. The cause is patients with dentinal dysplasia requires a multidisciplinary
    believed to be an environmental trigger, which results in mis- approach.
    directed immune response in people genetically susceptible.
    There is no cure for SLE. It is mainly treated with immunosup- CPP291 - ORAL CONDITIONS OF CAN-
    pressants, aiming to keep symptoms under control. Herein we CER PATIENTS ASSOCIATED WITH DIA-
    report a case of a female patient who presented an erythematous BETES AND ARTERIAL HYPERTENSION: CASE REPORT.
    ulcerative lesion surrounded by white threads in the palate. ERICA DA SILVA CARVALHO, GIULY MAIARA BARBOSA
    Incisional biopsy was made and microscopically was observed a ARIZA, ANGELA MONTEIRO, BARBARA MOURA VIGAS,
    lichenoid mucositis with a deep and perivascular inflammatory LIA MIZOBE ONO, EDUARDO J.S. HONORATO, LIONEI
    infiltrate. Also, basement membrane was clearly demonstrated by NOBRE CABRAL.
    PAS-stained sections. The final diagnosis was systemic lupus A 68-year-old female patient, with vitiligo, attended to the
    erythematosus with oral involvement. SLE is uncommon and hospital for breast cancer treatment. Also presented hypertension
    should be considered on the differential diagnosis of oral ulcer- and diabetes. During the clinical oral exam ICU were observed
    ative lesion in women. dark stains in the dorsum of the tongue, lingual fissures and
    lip-dryness. Also diagnosed has drug pigmentation with organic
    CPP289 - PERIPHERAL OSSIFYING FI- material. The treatment consist in oral sanitation with 0.12%
    BROMA INDUCED BY FOREIGN BODY digluconate chlorhexidine, followed by tongues crape with small
    IN PATIENT WITH SPECIAL NEEDS. GIEYSE NOGUEIRA spoon to remove the crust. In the fissures were used manipulated
    DE OLIVEIRA, TIAGO NOVAES PINHEIRO, LIONEY paste containing: VEGELIP, triamcinolone 10%/1g, associated
    NOBRE CABRAL, ANTÔNIO VASCONCELOS, II, ANA with the use of laser with low intensity. Was used artificial saliva
    CARLA PIMENTEL, JÉSSICA BARBOSA. to xerostomia and dexpantenol to the lip-dryness. The treatment
    The peripheral ossifying fibroma (POF) is considered a was finished in 5 days, 2 sessions with an interval of 12 hours
    borderline lesion from reactive to benign neoplastic nature. The resulting in regression of the case. Between the other 2 diseases,
    present study aims to report a case of POF related to the presence the hypertension influence more in a negative way the CA
    of a strange body in a patient with intellectual disabilities. A 38- treatment
    year-old male patient, leucoderma, was referred to the oral
    medicine service presenting with a pediculated nodule associated CPP292 - ORAL SYPHILIS IN A YOUNG
    with the inserted gingiva of tooth 21 with type II mobility. The PATIENT: A CASE REPORT. INGRID DA
    lesion presented normal coloration, bleeding on touch, asymp- SILVA SANTOS, VITOR BONETTI VALENTE, SOLANGE
    tomatic and well-defined borders. Excisional biopsy was per- PIRES D’ÁVILA, KELLEN CRISTINE TJIOE, ÉDER
    formed, and during the procedure it was found a foreign body RICARDO BIASOLI, GLAUCO ISSAMU MIYAHARA,
    similar to a popcorn husk, interfacing the base of the lesion with DANIEL GALERA BERNABÉ.
    the tooth cervical region. All tissue was submitted to histopath- Syphilis is a sexually transmitted disease caused by Trepo-
    ologic evaluation, concluding the diagnosis of POF. After 2 nema pallidum. A 23-year-old female patient was referred to the
    months of follow-up, the patient did not present recurrence. The clinic with multiple oral lesions 2 months ago. Her medical history
    association of the foreign body with the lesion reinforces the revealed that initially oral lesions were treated as pharyngitis by
    reactive nature of the POF. otolaryngologist with no favorable improvement of lesions. She
    also presented skin lesions, which were diagnosed as pityriasis by
    CPP290 - PREMATURE EXFOLIATION OF dermatologist. Intraoral examination showed erosive lesions and
    BOTH DECIDOUS AND PERMANENT mucous patches on the bilateral lip commissures, palate and border
    TEETH: A CASE REPORT. LILIANA APARECIDA PIMENTA of the tongue. Initially, immuno-mediated diseases were sus-
    DE BARROS, LUCIANA FARIA SANGLARD, MARIA pected, but hematologic tests were negative. However, non-tre-
    HELENA MONTEIRO DE BARROS MIOTTO, MARCELO ponemic test Venereal Disease Research Laboratory (VDRL) was
    PEÇANHA, SÉRGIO LINS DE AZEVEDO VAZ, TÂNIA reagent, therefore, syphilis was hypothesized. Biopsy was per-
    REGINA GRÃO VELLOSO, DANIELLE RESENDE formed and histopathologic aspects were suggestive of syphilis.
    CAMISASCA. Treponemic test fluorescent treponemal antibody-absorption
    A rare case of premature exfoliation of both deciduous and (FTA-ABS) was positive and secondary syphilis was confirmed.
    permanent dentitions is described. A 6-year-old white male pa- The treatment consisted of penicillin G benzathine for 3 weeks.
    tient presented at the Children Dental Clinic because of prema- After 6 months of follow-up, clinical and serological exams did
    ture loss of deciduous teeth. His mother reported difficulties in not show any sign of the disease.
    social interaction. Body weight and height were compatible with
    his age. He had been evaluated by a geneticist who suggested CPP293 - NASOPALATINE DUCT CYST:
    aggressive periodontitis as a probable diagnosis. Biochemical TREATMENT AND REHABILITATION.
    analysis revealed minor alterations. A very thin mandibular arch EVELYN ESTEFANI CRISTALDO, NELSON LUIS
    was observed, with only the first molars erupted in both arches. BARBOSA REBELLATO, PAOLA FERNANDA COTAIT DE
    Panoramic radiographs showed underdeveloped roots, narrow LUCAS CORSO, RICARDO PASQUINI FILHO, RAFAELA
    pulp chambers and absence of a few permanent teeth. Primary CRISTINA COSTA CARLOS, DELSON JOÃO DA COSTA.
    exfoliated teeth were sent to histopathologic analysis and The nasopalatine duct cyst is a non-odontogenic cyst origi-
    revealed formation of abnormal dentin. Dentin dysplasia type I nated from the reminiscents of the nasopalatine duct, which is
    was the diagnosis established. A complete over denture was most common in young adults. The aim of this case report will be
    made under the guidance of prosthodontist. Diagnosis should to show the case of a 41-year-old female patient that presented a

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