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1.
Int. j. odontostomatol. (Print) ; 13(4): 446-451, dic. 2019. tab, graf
Artículo en Español | LILACS | ID: biblio-1056483

RESUMEN

RESUMEN: Las papilas fungiformes pigmentadas de la lengua, cuyas siglas son PFPT, del inglés Pigmented fungiform papillae of the tongue, es una condición asintomática, no progresiva que se presenta en personas de piel oscura, en las cuales las papilas fungiformes cambian de su color rosado natural, a una gama de café a negro. El objetivo de nuestro estudio es reportar y describir las caractetísticas clínicas, dermatoscópicas e histológicas de la PFPT por primera vez en una serie de pacientes ecuatorianos. Estudio prospectivo simple en el Centro de Especialidades Dermatológicas Garzón, período de dos años. El criterio de inclusión fue cambio de coloración a nivel lingual, se recolectaron datos demográficos, clínicos; fotografías, dermatoscopía, y biopsia, para tinción con hematoxilina-eosina y Fontana-Mason. Examinamos 8.640 pacientres, 15 (12 mujeres, 3 varones) fueron diagnosticados de PFPT. La edad promedio fue 31 años, todos fueron mestizos, con fototipo de piel predominante III y IV. El tiempo de evolución promedio en años fue 5,8. Ninguno tuvo antescedentes familiares o personales relacionados a la patología. La evaluación clínica demostró que el patrón de distribución de acuerdo a la clasificación de Holzwanger en la gran mayoría fue tipo II (13/15). En todos los casos la dermatoscopía y la histología fueron específicas demostrando hallazgos típicos y comprobatorios de PFPT.


ABSTRACT: The pigmented fungiform papillae of the tongue, whose acronyms are PFPT, of the English Pigmented fungiform papillae of the tongue, is an asymptomatic, nonprogressive condition that occurs in dark-skinned people, in which the fungiform papillae change their color natural pink, to a range of brown to black. The aim of our study is to report and describe the clinical, dermatoscopic and histological characteristics of the PFPT for the first time in a series of Ecuadorian patients. A simple prospective study at the Garzón Dermatological Specialty Center, a two-year period. The inclusion criteria was lingual change of color, demographic, clinical data were collected; photographs, dermatoscopy, and biopsy, for staining with hematoxylin-eosin and FontanaMason. We examined 8,640 patients, 15 (12 women, 3 men) were diagnosed with PFTP. The range of age was 31 years, all were mestizos, with skin phototype predominant III and IV. The range of evolution time in years was 5.8. None had family or personal precedents related to the pathology. The clinical evaluation showed that the pattern of distribution according to the Holzwanger classification in the great majority was type II (13/15). In all cases, the dermatoscopy and histology were specific, demonstrating typical and evidential findings of PFPT.


Asunto(s)
Humanos , Masculino , Femenino , Niño , Adolescente , Adulto , Persona de Mediana Edad , Neoplasias Cutáneas , Papilas Gustativas/patología , Enfermedades de la Lengua/patología , Hiperpigmentación/patología , Melaninas/análisis , Enfermedades de la Lengua/etiología , Biopsia , Estudios Prospectivos , Micosis Fungoide/complicaciones , Hiperpigmentación/etiología , Dermoscopía/métodos , Colorantes , Ecuador
2.
Medicina (B.Aires) ; 79(6): 509-512, dic. 2019. ilus
Artículo en Español | LILACS | ID: biblio-1056761

RESUMEN

La arteritis de células gigantes es una vasculitis sistémica que compromete arterias de mediano y gran calibre, principalmente la arteria aorta y sus ramas. Su prevalencia es mayor en mujeres a partir de los 50 años, típicamente se manifiesta con fiebre, claudicación mandibular, cefalea, hiperestesia del cuero cabelludo y pérdida de la visión con neuropatía óptica isquémica anterior, en una minoría de casos aparecen síntomas menos frecuentes que dificultan y retrasan el diagnóstico. Se presenta el caso de una mujer de 76 años que consultó por dolor en la cavidad bucal con edema lingual y en cuello de 48 horas de evolución asociado a cefalea el mes previo. En el examen físico presentaba signos clínicos de isquemia lingual, por lo que se consideró como diagnóstico presuntivo compromiso isquémico por arteritis de células gigantes, e inició tratamiento con corticoides sistémicos realizándose una biopsia de arteria temporal que evidenció infiltrado linfocitario panparietal con engrosamiento de la túnica íntima y hallazgos compatibles con panarteritis. La arteritis de células gigantes debe ser sospechada en pacientes con manifestaciones de isquemia lingual, iniciándose en forma precoz el tratamiento para evitar complicaciones irreversibles.


Giant cell arteritis is a systemic vasculitis that affects arteries of medium and large caliber, mainly the aorta artery and its main branches. It is more frequent in women older than 50 years. The most common symptoms are fever, jaw claudication, headache, hyperesthesia of the scalp and loss of vision with anterior ischemic optic nerve disease. But, in a minority of cases, less frequent symptoms are observed that delay and make more difficult the diagnosis. Here, we present the case of a 76-year-old woman who came to our consultation having pain in the oral cavity and presenting tongue and neck edema for 48 hours. She had also suffered from headaches during the previous month. Because the physical examination showed clinical signs of lingual ischemia, a presumptive diagnosis of ischemic involvement due to giant cell arteritis was considered. She started a treatment with systemic corticosteroids and a temporal artery biopsy was performed. We conclude, that giant cell arteritis should be suspected in patients presenting lingual ischemia symptoms in order to start the specific treatment early enough to avoid irreversible complications.


Asunto(s)
Humanos , Femenino , Anciano , Arteritis de Células Gigantes/patología , Enfermedades de la Lengua/patología , Arteritis de Células Gigantes/diagnóstico , Arteritis de Células Gigantes/tratamiento farmacológico , Enfermedades de la Lengua/diagnóstico , Enfermedades de la Lengua/tratamiento farmacológico , Diagnóstico Diferencial , Glucocorticoides/uso terapéutico , Necrosis
3.
Artículo en Inglés | LILACS, BBO | ID: biblio-1056865

RESUMEN

Abstract Objective: To examine the relationship between the level of glycemic control and coated tongue in type 2 diabetes mellitus patients with xerostomia. Material and Methods: This study was an analytical survey and involved 64 type 2 diabetes mellitus patients, aged between 17 to 65 years old with 34 males and 30 females. Diagnosis of diabetes mellitus was determined from the patient's medical records. The level of glycemic control was obtained from the patient's last blood sugar examination. Xerostomia was diagnosed with a questionnaire, while coated tongue diagnosis based on clinical features and the severity of coated tongue was assessed using the Kojima index Results: There was a significant relationship between the level of glycemic control and coated tongue (p=0.0026) in type 2 diabetes mellitus patients with xerostomia. Moreover, there was a significant relationship between the level of glycemic control and the severity of the coated tongue (p=0.001). Specifically, poor glycemic control was associated with a higher occurrence of the coated tongue as well as more severe tongue coating Conclusion: There was a significant relationship between the level of glycemic control in and coated tongue in type 2 diabetes mellitus patients with xerostomia. Therefore, diabetes mellitus patients should control their level of glycemic control to prevent the oral complication of the disease.


Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Persona de Mediana Edad , Anciano , Enfermedades de la Lengua/patología , Xerostomía/diagnóstico , Diabetes Mellitus/patología , Diabetes Mellitus Tipo 2/patología , Control Glucémico , Registros Médicos , Encuestas y Cuestionarios , Interpretación Estadística de Datos , Índice Glucémico , Estudios Observacionales como Asunto/métodos , Indonesia/epidemiología
5.
Clin. biomed. res ; 36(3): 168-171, 2016. ilus
Artículo en Inglés | LILACS | ID: biblio-831726

RESUMEN

Gangrene of the tongue is a condition rarely described in the literature. It generally occurs in association with temporal arteritis and other vasculitides. We described a rare case of tongue necrosis associated with oropharyngeal carcinoma. A 67-male patient, previously submitted to exclusive radiotherapy for a squamous cell carcinoma of the tonsillar region, was admitted to our service with high dysphagia. Computed tomography showed circumferential swelling of the oropharynx, with areas of diffuse contrast uptake and significant reduction of the vascular flow at this level, especially venous return. About 6 months after the onset of symptoms, he was submitted to an urgent tracheostomy for airway obstruction. Then, about 1 month after tracheotomy, the neck skin became ecchymotic, congested, and he started with profuse oropharyngeal bleeding and congestion and thrombosis signs in the tongue. To our knowledge, this entity has not been yet described in the literature (AU)


Asunto(s)
Humanos , Masculino , Anciano , Necrosis , Neoplasias Orofaríngeas , Enfermedades de la Lengua/patología , Resultado Fatal , Lengua/patología
6.
An. bras. dermatol ; 90(3,supl.1): 226-228, May-June 2015. ilus
Artículo en Inglés | LILACS | ID: lil-755744

RESUMEN

Abstract

The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history. Recurrent bleeding, hypoxemia, congestive heart failure, portosystemic encephalopathy, and symptoms related to angiodysplasia of the central nervous system may occur. Since the treatment is based on supportive measures, early recognition is of utmost importance. This article reports the case of a 53-year-old male patient who presented telangiectasias on fingers, oral cavity and nasal mucosa for 10 years, with a history of recurrent epistaxis of varying severity since childhood. Mother, sister and daughter have similar lesions.

.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Epistaxis/patología , Enfermedades Genéticas Congénitas/patología , Telangiectasia Hemorrágica Hereditaria/patología , Enfermedades del Esófago/patología , Síndrome , Gastropatías/patología , Enfermedades de la Lengua/patología
7.
An. bras. dermatol ; 90(3,supl.1): 88-90, May-June 2015. tab, ilus
Artículo en Inglés | LILACS | ID: lil-755796

RESUMEN

Abstract

Eosinophilic ulcer of the oral mucosa is a rare, self-limiting, chronic and benign lesion of unknown pathogenesis that affects the oral mucosa. We present the case of a 65 year-old Caucasian female with a fivemonth history of a painful ulcer on the lateral side of her tongue. The ulcer was not adhered to the underlying structures and there was no evidence of regional lymph node involvement. Laboratory examinations and X-rays revealed no abnormalities. Topical treatments had been performed without any improvement. Histopathological examination showed an ulcerated surface and mixed inflammatory infiltrate with several eosinophils extending into the mucosa and submucosa. No cellular atypia was observed. Based on the patient-s history and mucosal biopsy, a final diagnosis of eosinophilic ulcer of the oral mucosa was made.

.


Asunto(s)
Anciano , Femenino , Humanos , Eosinofilia/patología , Úlceras Bucales/patología , Enfermedades de la Lengua/patología , Biopsia , Diagnóstico Diferencial , Mucosa Bucal/patología
8.
Audiol., Commun. res ; 19(4): 375-379, Oct-Dec/2014. tab
Artículo en Portugués | LILACS | ID: lil-732234

RESUMEN

Objetivo Caracterizar a pressão da língua em idosos. Métodos Estudo transversal, com a participação de 45 idosos, de 61 a 96 anos, sendo 34 (75,6%) do gênero feminino e 11 (24,4%) do masculino, sem distúrbios neurológicos e cognitivos, sem histórico de câncer de cabeça e pescoço e de procedimento radioterápico. Consistiu na aplicação de questionário, com registro da presença ou ausência de queixa de problemas na deglutição, seguido da avaliação miofuncional orofacial, enfocando a mobilidade e tensão de língua. Para a mensuração da pressão da língua, foi utilizado o Iowa Oral Performance Instrument (IOPI). A análise dos dados foi descritiva, com nível de significância de 5%. Resultados A média do pico pressórico foi de 44,6 KPa (±16), com os valores mínimo e máximo entre 9 e 88 KPa. Houve correlação moderada negativa entre pico pressórico e idade. Os longevos apresentaram a menor média de pico pressórico e inferior ao padrão de normalidade. Houve diferença entre a média de pico pressórico e uso de próteses, tensão de língua e mobilidade de língua no estalo. Conclusão Houve diminuição moderada do pico pressórico da língua com o aumento da idade e redução pressórica com o decréscimo da tensão da língua e de sua mobilidade no estalo. Em contrapartida, os valores de pico foram maiores nos idosos que utilizam próteses dentárias, quando comparados aos que destas não fazem uso. .


Purpose To characterize tongue pressure in elderly individuals. Methods This was a cross-sectional study involving 45 individuals aged between 61 and 96 years old (34 [75.6%] women; 11 [24.4%] men) with no neurological or cognitive disorders, no history of head or neck cancer, and no history of radiotherapy. The subjects were surveyed with a questionnaire that recorded the presence or absence of complaints about swallowing problems and an orofacial myofunctional evaluation, which examined the movement and tension of the tongue. The Iowa Oral Performance Instrument (IOPI) was used to measure tongue pressure. The data analysis was descriptive, with significance set at the 5% level. Results The mean pressure peak was 44.6 kPa (±16), with minimum and maximum values of 9 and 88 kPa, respectively. Pressure peak and age were moderately and negatively correlated. The oldest subject had the lowest average pressure peak, which was less than the normal range. The mean pressure peak differed according to the use of dentures, tongue pressure, and tongue mobility during clicking. Conclusion The pressure peak and the pressure of the tongue decreased moderately with increasing age, decreasing tongue tension, and mobility during clicking. In contrast, the pressure peak values were higher in the elderly who used dentures than those who did not. .


Asunto(s)
Humanos , Masculino , Femenino , Persona de Mediana Edad , Anciano , Anciano de 80 o más Años , Trastornos de Deglución/diagnóstico , Prótesis Dental , Dolor Facial/diagnóstico , Enfermedades de la Lengua/patología , Distribución por Edad y Sexo , Estudios Transversales , Disartria/diagnóstico , Salud del Anciano
9.
An. bras. dermatol ; 89(4): 679-680, Jul-Aug/2014. graf
Artículo en Inglés | LILACS | ID: lil-715548

RESUMEN

Rendu-Osler-Weber Syndrome also known as Hereditary Hemorrhagic Telangiectasia is a rare systemic fibrovascular dysplasia, with dominant autosomal inheritance. It is characterized by recurrent epistaxis, mucocutaneous telangiectasia, visceral arteriovenous malformation and positive family history. There may be hematologic, neurologic, dermatologic and gastrointestinal complications. Therapy is supportive and aimed at preventing complications. In this article we report a case of Rendu-Osler-Weber in a 64 year-old man, with history of mucocutaneous telangiectasia since the third decade of life, recurrent epistaxis, positive family history and vascular ectasia in the gastrointestinal tract.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Telangiectasia Hemorrágica Hereditaria/patología , Enfermedades de la Lengua/patología , Síndrome , Telangiectasia Hemorrágica Hereditaria/complicaciones , Células Endoteliales/patología
11.
Artículo en Inglés | IMSEAR | ID: sea-157567

RESUMEN

Context: Tongue lesions are quite common and affect both genders and all age groups. However, very few studies concentrate on the histopathological spectrum of tongue lesions, usually including them as a part of oral cavity lesions. No such study has been published from the newly formed state of Uttarakhand. Aim: A retrospective review of histopathology of various types of tongue lesions in different age groups of both genders, amongst cases reported in the department of pathology. Methods and Materials: Study included a total of 121 cases of tongue lesions reported in the histopathology section over a duration of five years, from July 2004 to June 2009. Result: In this study, the most common lesions were malignant (58.7%), followed by benign lesions (33%) and pre-malignant lesions (8.3%). The most common site for tongue lesions was base of tongue (52.8%). Common age groups affected were 41- 50 years (27.2%) and 51-60 years (28.0%). The most common clinical presentation was growth and induration. Overall males were affected more than females; with Male:Female ratio of 3.3:1. Conclusions: The commonest tongue lesion in this study was moderately differentiated squamous cell carcinoma among the malignant lesions whereas chronic inflammation was the commonest out of non-malignant lesions. Tongue may show some less common tumours like schwannoma and hemangioma etc.


Asunto(s)
Adulto , Femenino , Humanos , Masculino , Persona de Mediana Edad , Patología , Enfermedades de la Lengua/diagnóstico , Enfermedades de la Lengua/epidemiología , Enfermedades de la Lengua/patología , Neoplasias de la Lengua/diagnóstico , Neoplasias de la Lengua/epidemiología , Neoplasias de la Lengua/patología
12.
J. oral res. (Impresa) ; 2(1): 28-30, abr. 2013. ilus
Artículo en Español | LILACS | ID: lil-708323

RESUMEN

El osteoma lingual (coristoma óseo lingual) es una alteración del desarrollo poco común, con menos de 100 casos reportados mundialmente. La localización más frecuente de esta lesión es la cara dorsal de la lengua. Su etiología no es completamente clara. Debido a su escasa incidencia, reportamos un nuevo caso, en una paciente de sexo femenino de 12 años de edad. En este artículo también se revisará la epidemiología, histología y patogénesis de esta condición.


Lingual osteoma (lingual osseous choristoma) is a rare condition, with fewer than 100 cases reported. The most common location of this lesion is the dorsal surface of the tongue. Because of its low incidence, we present a new case that occurred in a 12 years old woman. This article also review the epidemiology, histology and pathogenesis of this condition.


Asunto(s)
Humanos , Femenino , Niño , Huesos , Coristoma/patología , Enfermedades de la Lengua/patología , Osteoma
14.
Rev. chil. dermatol ; 28(3): 300-304, 2012. ilus, tab
Artículo en Español | LILACS | ID: lil-768973

RESUMEN

Las glándulas de Blandin-Nuhn son un grupo de pequeñas glándulas salivales mucoserosas, ubicadas en el espesor de los haces musculares de la zona anterior de la cara ventral de la lengua. Los mucoceles de las glándulas de Blandin-Nuhn son poco frecuentes. Se revisa la literatura y se presentan dos casos de mucocele de las glándulas de Blandin-Nuhn, ambos casos eran lesiones exofíticas, indoloras, una de ellas asociada a trauma. Los mucoceles de las glándulas salivales linguales anteriores deben ser resecados hasta el plano muscular para evitar la recidiva. Como esta lesión puede ser confundida con otras patologías, se recomienda su estudio histopatológico para evitar diagnósticos errados.


The Blandin-Nuhn glands are a small group of mucous serous salivary glands, located in the thickness of the muscle bundles of the anterior ventral side of the tongue. Mucocele of the glands of Blandin-Nuhn has been reported as unusual. We review the literature and present two cases of mucocele of the glands of Blandin-Nuhn, both cases were exophytic lesions, painless, one associated with trauma. Mucoceles of the salivary glands should be resected up to the muscular plane to avoid recurrence. Because this lesion may be confused with other diseases, it is recommended an histopathological exam to avoid misdiagnosis.


Asunto(s)
Humanos , Masculino , Adulto , Femenino , Enfermedades de la Lengua/patología , Enfermedades de las Glándulas Salivales/patología , Glándulas Salivales Menores/patología , Mucocele/patología , Diagnóstico Diferencial , Enfermedades de la Lengua/diagnóstico , Enfermedades de la Lengua/terapia , Enfermedades de las Glándulas Salivales/diagnóstico , Enfermedades de las Glándulas Salivales/terapia , Mucocele/diagnóstico , Mucocele/terapia
15.
Arq. int. otorrinolaringol. (Impr.) ; 15(3): 388-391, jul.-set. 2011. ilus
Artículo en Portugués | LILACS | ID: lil-606465

RESUMEN

INTRODUÇÃO: A Síndrome de Richner-Hanhart se caracteriza pela ausência em grau variável de porções distais de uma ou mais extremidades, associada à micrognasia e microglossia severa. A etiologia desta rara síndrome permanece desconhecida. RELATO DE CASO: Neste artigo relatamos o caso de um paciente com Síndrome de Richner-Hanhart que apresentava ausência de terço anterior da língua, micrognatia, malformações dos pododáctilos e quirodáctilos, de pés e mãos, além de desvio de septo nasal para esquerda. COMENTÁRIOS FINAIS: O tratamento consiste em dieta com restrição de tirosina e acompanhamento contínuo com otorrinolaringologista e fisioterapeuta.


INTRODUCTION: Richner-Hanhart Syndrome is characterized by the absence in a variable degree of distal portions of one or more extremities, in association with micrognathia and severe microglossia. The etiology of this infrequent syndrome remains unknown. CASE REPORT: In this article, we report the case of a patient with Richner-Hanhart Syndrome, who showed an absence of the back third of the tongue, micrognathia, malformation of fingers and toes, as well as nasal septum deviation to the left. FINAL COMMENTS: The treatment comprises a tyrosine-restricted diet together with a continuous follow-up with an otorhinolaryngologist and a physiotherapist.


Asunto(s)
Humanos , Masculino , Femenino , Lactante , Carcinoma Hepatocelular , Conservantes de Alimentos , Enfermedades de la Lengua/etiología , Enfermedades de la Lengua/patología , Neoplasias Hepáticas , Deformidades Congénitas de las Extremidades Inferiores , Deformidades Congénitas de las Extremidades Superiores
17.
Artículo en Inglés | IMSEAR | ID: sea-139764

RESUMEN

Background: Oral lichen planus is an inflammatory chronic disease with an autimmune pathogenesis and unknown etiology that affects oral mucosa, with or without the involvement of the skin and other mucous membranes. The principal histological characteristics are the degeneration of the basal cell layer and the abnormal infiltration of inflammatory cells into the subepithelial layer of connective tissue. Objectives: This study is aimed to appraise if lingual lichen planus (LLP) is sustained by alteration of the oral microcirculation and if this abnormal vascularisation increases the degeneration of basal keratinocytes and the disruption of the basement membrane. Materials and Methods: Fifteen patients with a histological diagnosis of LLP with higher degree of degeneration of the basement membrane, fifteen LLP patients with lower degree of basement membrane (BM) degeneration and fifteen healthy patients were included in the study. The microcirculation of the left margin of the lingual mucosa of all the patients and subjects was analysed with the videocapillaroscopy. The following parameters were analyzed on each capillaroscopic image: c0 apillary loop length, loop diameter, and capillary density. The results obtained by videocapillaroscopy software were subjected to statistical analysis using Mann Whitney U-test (P < 0.001). Statistical analysis was performed using PAST software, v. 1.53. Results: Capillary density, loop length, and total diameter showed statistically significant differences between LLP patients with histologically lower degree of BM degeneration and healthy subjects and a meaningful significant difference between LLP patients with higher degree of BM degeneration. Conclusions: A remarkable increase in capillary density was showed by videocapillaroscopic exam. The increased value of the density could be associated with angiogenesis mechanism and it could be an indicator of the evolutionary condition of LLP. Videocapillaroscopy may be useful for the evaluation of the evolution or regression of the disease.


Asunto(s)
Adulto , Anciano , Membrana Basal/patología , Capilares/patología , Capilares/fisiopatología , Tejido Conectivo/patología , Células Epiteliales/patología , Epitelio/patología , Femenino , Humanos , Queratinocitos/patología , Liquen Plano Oral/patología , Liquen Plano Oral/fisiopatología , Masculino , Microcirculación/fisiología , Angioscopía Microscópica , Microscopía por Video , Persona de Mediana Edad , Mucosa Bucal/irrigación sanguínea , Mucosa Bucal/patología , Lengua/irrigación sanguínea , Lengua/patología , Enfermedades de la Lengua/patología , Enfermedades de la Lengua/fisiopatología
18.
Artículo en Inglés | IMSEAR | ID: sea-139718

RESUMEN

Acute traumatic ulcerations and granulomas of the oral mucosa may result from physical damage via sharp foodstuffs, accidental biting, or talking. Most ulcerations heal within days. Others become chronic, reactive, and exophytic. A histopathologically unique type of chronic traumatic ulceration is the traumatic ulcerative granuloma with stromal eosinophilia (TUGSE). TUGSE exhibits a deep "pseudoinvasive" inflammatory reaction. This lesion may occur under the tongue in infants as a result of chronic mucosal trauma caused by mandibular anterior primary teeth during nursing and is termed Riga-Fede disease (RFD). The clinical presentation many resemble squamous cell carcinoma causing concern. RFD, although not uncommon, is not frequently reported. Thus, dental practitioners are unfamiliar with such lesions. We present a large Riga-Fede lesion in an infant along with the clinical management.


Asunto(s)
Enfermedad Crónica , Diagnóstico Diferencial , Granuloma/patología , Humanos , Lactante , Masculino , Úlceras Bucales/diagnóstico , Úlceras Bucales/patología , Lengua/lesiones , Enfermedades de la Lengua/diagnóstico , Enfermedades de la Lengua/patología , Erupción Dental
20.
Indian J Pathol Microbiol ; 2008 Jan-Mar; 51(1): 65-6
Artículo en Inglés | IMSEAR | ID: sea-74704

RESUMEN

Primary tuberculosis of tongue is very rare with unusual presentation creating a diagnostic dilemma. We report a case of primary tuberculosis of tongue in a 49-year-old female patient. Tuberculosis was not suspected clinically and there was no other focus elsewhere in the body. Fine needle aspiration cytology was attempted but was inconclusive. The diagnosis was made after histopathological examination.


Asunto(s)
Biopsia con Aguja Fina , Femenino , Histocitoquímica , Humanos , Persona de Mediana Edad , Enfermedades de la Lengua/patología , Tuberculosis/diagnóstico
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