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Biomedical subjects

J Risco

Publications and source records attributed to J Risco.

13 recordsLinked to original sources

[Submaxillary sialolithiasis due to Actinomyces israelii. A case report].

Actynomicosis of the submaxillary gland is a very uncommon infectious disease. In this article one case of submaxillary sialolithiasis by actynomices israelii in a young girl is presented. We discuss several aspects of its diagnosis and therapeutic possibilities and review the literature on the subject. We emphasize the interest and value of performing a microbacteriological, mineralogical and pathological study of the calculi.

Actinomycosis↗

Bone SPECT in cholesteatoma assessment.

Bone SPECT in cholesteatoma assessment. Single photon emission computed tomography (SPECT) is a procedure in nuclear medicine which enables bone lesions to be better assessed. Twenty patients with cholesteatoma were studied to assess the efficiency of SPECT in bone lesions produced by cholesteatoma. Every patient also had a middle ear computed tomography (CT) and underwent surgery and anatomopathologic examination. Results obtained by SPECT are compared to CT results. SPECT was positive in 15 cases of which 2 of them with a negative CT for bone erosion. Five cases were false negative, but 2 of them had contralateral ear pathology and in one case bone erosion was not found. We conclude that in some patients SPECT can be a complementary diagnostic procedure in cholesteatomatous bone lesions.

Adolescent↗

[In-depth study of the causes of sudden deafness. Physiopathological mechanisms and their reversal].

This article deals with an investigative work done by the AA. with the aim of determine the final cause of sudden sensorial deafness. Three causes are accepted as source of sudden deafness: viral infections, the tear away of labyrinthine membranes and the vascular theory. An increase in antibody titer suggest a viral origin. The labyrinthine membranes split has been observed at times when performing an exploratory tympanotomy. But circulatory troubles are hardly diagnosed, even with histopathological evidences of vascular upsets in temporal bones belonging to patients who suffered from an auditory stroke, because there are no diagnostic tests for "in vivo" control. Our intend is to investigate on the physiopathology of unforeseen deafness and also try to know the possible mechanisms of reversion of this calamitous pathology. We use, as investigative method of actual vascular changes in sudden deafness, the following; the speed analysis of the blood flow furnished by the A. labyrinthi through echography Doppler color transcranialis and angiography and magnetic resonance (Angio-MR). Both procedures are non invasive and harmless. We comment the findings of 13 patients. And find out, in 4 cases, an important trouble of the arterial vertebrobasilaris flow. The A. labyrinthi, a branch of the A. cerebelli inferior anterior (ACIA) and/or A. basilaris--rarely from the A. cerebelli inferior posterior (ACIP)--showed a heavy hypoplasy of these vessels, stenosis or complete blockage. In 2 of cases, 4 months later, a new exploration of the Doppler flow and angio-MR, was performed, and detected an improvement of the vertebrobasilar flow, in both instances. In those patients with an evident recovery of the hearing, it was attributed to these two compensatory mechanisms: 1) reversal of the flow at the level of cicle of Willis, at the expense of development of A. communicans posterior, and 2) cessation of the vertebral A. spasm and decrease of the vessel's tortuosity so improving the blood flow.

Aged↗

[Treatment and outcome of infantile cholesteatoma surgery].

Infantile Cholesteatoma has been lately the aim of a large number of papers dealing with its natural history and optimal treatment. The outcome of 26 cases of ear surgery, done between 1990 and 1991, are reviewed. The etiology of Cholesteatoma was congenital in 2 cases, iatrogenic in an other one and unknown for the remainder (88%). Fifteen (15) closed surgical procedures and 11 open were carry out, achieving global removal of lesions in 76 percent of cases. Ninety-one (91%) of open tympanoplasties and 66 percent of closed procedures. Six cases evolved to recidivation (and later reoperatively reconverted in open cases) owing either to the erosion of the ossicular chain or encroachment of the recessus. Reconstructions of the ossicular chain was undertaken in 61.5 percent of cases and the hearing preserved in all instances and improved in 35 percent of reconstructions.

Adolescent↗

Adenoid cystic carcinoma initially diagnosed and treated as hemangioma.

Adenoid cystic carcinoma initially diagnosed and treated as hemangioma. A case diagnosed as having a hemangioma of the soft palate according to clinical and arteriographic findings is discussed. Recurrence appeared one year after embolization. Arteriography showed no vascular lesion and histopathologic study revealed an adenoid cystic carcinoma. It is stated that imaging studies may be insufficient.

Carcinoma, Adenoid Cystic↗

[Mikulicz disease as the beginning of AIDS].

Major salivary lymphoepithelial lesions accounted for less than 3 percent of all benign parotid tumors, prior to AIDS acquaintance. Defined as the presence of enlargement of one or more salivary glands and, in some cases, with diminished salivary function. The paper present the case of an acquired immunodeficiency syndrome starting as a Mikulicz's disease. Reviewed the medical literature and treatment options.

Acquired Immunodeficiency Syndrome↗

[Jugular phlebectasia. Apropos a case].

We present a case of 6-years-old male with an internal jugular phlebectasia, diagnosed at our Hospital. Review of the bibliography, and complementary examination, like doppler, echography and digital intravenous angiography subtraction (DIVAS) was made.

Angiography, Digital Subtraction↗

[Non-syndromic familial deafness. Review and genetic study].

Many cases of hearing impairment are of genetic origin. Non-syndromic recessive transmission is the most frequent form. A genetic study was made of cases of non-syndromic familial hearing impairment seen in our service. The pattern of Mendelian inheritance was studied in the disorders associated with deafness. Four families had non-syndromic deafness and autosomal inheritance (3 dominant and one recessive) and one had a probable sex-linked inheritance. Genetic counseling was given and guidelines were created after reviewing the literature.

Adolescent↗

[Otoneurological manifestations of basilar dolicoectasia. A report of six cases].

Megadolichobasilar is a vascular anomaly consisting of widening and elongation of the basilar artery. It is rare and may produce otoneurological manifestations such as vertigo, sudden deafness, trigeminal neuralgia, and facial spasm or palsy. Six cases of megadolichobasilar diagnosed by magnetic resonance angiography are reported and their pathogenesis is discussed.

Adult↗