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1.
Rev. cuba. cir ; 58(3): e684, jul.-set. 2019. graf
Article in Spanish | LILACS, CUMED | ID: biblio-1098979

ABSTRACT

RESUMEN Se presenta el caso de un paciente de 21 años de edad que refiere aumento paulatino del escroto de varios meses de evolución, sin dolor u otros síntomas. Con el objetivo de exponer una lesión benigna paratesticular clasificada como, tumor fibroso de la túnica vaginal, se practicó una escrototomía con toma de biopsia, exéresis de la tumoración y se conservó el testículo. El tejido fibroso fue puesto en evidencia con la biopsia intraoperatoria, posteriormente la histopatología hizo el diagnóstico de tumor fibroso. La orquiectomía es posible evitarla cuando nos encontramos ante lesiones paratesticulares que son benignas en la mayoría de los casos(AU)


ABSTRACT We present the case of a 21-year-old patient who reports a gradual increase in the scrotum of several months of evolution, without pain or other symptoms. In order to expose a benign paratesticular lesion classified as fibrous tumor of the vaginal tunic, a scrototomy was performed with biopsy, excision of the tumor and the testicle was preserved. The fibrous tissue was revealed with the intraoperative biopsy, later histopathology made the diagnosis of fibrous tumor. Orchiectomy can be avoided when we are faced with paratesticular lesions that are benign in most cases(AU)


Subject(s)
Humans , Male , Adult , Testis/surgery , Solitary Fibrous Tumor, Pleural/etiology , Solitary Fibrous Tumor, Pleural/pathology
2.
Acta Chir Belg ; 116(6): 386-387, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27376978

ABSTRACT

Doege-Potter syndrome is a paraneoplastic syndrome characterized by tumor-associated hypoglycemia secondary to a solitary fibrous tumor of the pleura. We present a case of an 84-year-old man, who presented with acute mental confusion and therapy-resistant hypoglycemia. Diagnostic imaging revealed a large sharply defined pleural tumor based on the left diaphragm, after surgical resection the diagnosis was made of a malignant solitary fibrous tumor of the pleura and restoration of the glucose homeostasis was observed.


Subject(s)
Kidney Diseases/congenital , Kidney/abnormalities , Pleural Neoplasms/etiology , Solitary Fibrous Tumor, Pleural/etiology , Aged, 80 and over , Congenital Abnormalities , Diagnosis, Differential , Humans , Kidney Diseases/complications , Male , Pleural Neoplasms/diagnosis , Positron-Emission Tomography , Solitary Fibrous Tumor, Pleural/diagnosis , Tomography, X-Ray Computed
3.
Gac. méd. espirit ; 16(1): 40-49, ene.-abr. 2014.
Article in Spanish | LILACS | ID: lil-705626

ABSTRACT

Fundamento: los tumores fibrosos localizados de pleura son raros, de etiología incierta; la mayoría de los pacientes con esta enfermedad sobrepasan la quinta década de vida y más de la mitad están asintomáticos al diagnóstico, principalmente cuando los tumores son pequeños. Objetivo: describir el caso de una paciente con tumor fibroso localizado de pleura que, por su edad, sintomatología y por las características histológicas del tumor, representa una situación clínica infrecuente, con dificultades para el diagnóstico. Presentación de caso: mujer saludable, de 39 años, con dolor tóraco-lumbar persistente, de un año de evolución; en radiografía de tórax se visualizó imagen retro cardíaca izquierda corroborada por tomografía computarizada. Se realizó exéresis total de una masa de 4,8 cm, pedunculada, con origen en la pleura visceral, cuyo diagnóstico histopatológico fue un tumor fibroso localizado de pleura con características quísticas. Después de varios meses de seguimiento la paciente permanecía saludable y sin signos de recurrencia. Conclusiones: este caso constituye una forma infrecuente de presentación del tumor fibroso localizado de pleura por tratarse de una paciente menor de 40 años, con una sintomatología no frecuente y por el comportamiento benigno que ha tenido el tumor aunque presentó características quísticas.


Background: localized fibrous tumors of the pleura are rare, with uncertain etiology; most of the patients with this disease exceed the fifth decade of life and more than a half are without symptoms at the diagnosis, mainly when tumors are small. Objective: to describe a case of a female patient with a diagnosis of a localized fibrous tumor of pleura in which due to her age, the symptomatology and histological features of the tumor, it represents an infrequent clinical situation with difficulties for the diagnosis. Case presentation: a 39-year-old healthy woman with one year history of persistent thoracic lumbar pain; in chest radiography a left retrocardiac image was observed and it was corroborated by chest CT scan. Total exeresis was performed in a 4.8 cm mass, pedunculated, originating from the visceral pleura, whose histopathological diagnosis was a localized fibrous tumor of the pleura with cystic features. After several months of follow-up, the patient remained healthy and did not show recurrent signs. Conclusions: this case is an infrequent presentation of a localized fibrous tumor of the pleura for having been diagnosed in a patient under 40 years old, with an infrequent symptomatology and because the tumor has shown a benign behavior even with cystic features.


Subject(s)
Humans , Pleural Neoplasms/diagnosis , Solitary Fibrous Tumor, Pleural/etiology
4.
Eur J Cardiothorac Surg ; 41(3): 587-97, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22345180

ABSTRACT

Solitary fibrous tumours of the pleura are rare. They are mesenchymal in origin. Initially, they were described in the pleura, but lately they have been reported in many other sites. Although the majority of these tumours are benign, some of them are malignant. Their unpredictable clinical course is probably related to their histological and morphological characteristics. The benign tumours may remain unproblematic for several years before changing into a malignant form. In order to define more accurately the clinical behaviour, diagnosis, management and outcome of these rare tumours, we reviewed the literature with particular attention to clinical presentation, methods of diagnosis, treatment and outcome. Furthermore, a modified algorithm was proposed for the management of these tumours.


Subject(s)
Solitary Fibrous Tumor, Pleural/diagnosis , Algorithms , Diagnosis, Differential , Humans , Incidence , Magnetic Resonance Imaging , Positron-Emission Tomography , Prognosis , Solitary Fibrous Tumor, Pleural/epidemiology , Solitary Fibrous Tumor, Pleural/etiology , Solitary Fibrous Tumor, Pleural/therapy , Tomography, X-Ray Computed
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