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Biomedical subjects

S Asuar Aydillo

Publications and source records attributed to S Asuar Aydillo.

14 recordsLinked to original sources

[Hypernephroma in native kidney of patient with renal transplant].

The uremic patients, specially in periodic dialysis, may present bilateral kidneys cytes with high frequency. This pathology, known as acquired cyst renal disease, is found associated in its evolution with the emergence renal malignant disease. A patient who undergoing chronic dialysis and renal transplant subsequently developed an asymptomatic renal neoplasm. The epidemiological, clinical, diagnostic aspects and therapeutic of the acquired cysts renal and your association with renal cancer are analyzed.

Humans↗

[Solitary cerebral metastasis of a renal cell carcinoma].

The tumour dissemination to brain from renal cell carcinoma is a rare occurrence: generally, it's seen in advanced stages of the disease, such that occurred in our patient that indicated a poor prognosis. A lesion node, the size medle, located in the side left to brain, with of symptoms neurologic associated was found. Histological examination of the resection specimen revealed metastasis from a renal cell carcinoma.

Aged↗

[Giant inguinoscrotal bladder hernia].

Inguinoscrotal bladder hernia occur in 0.4 to 3% of general poblation, though massive hernia are much rare. We present a new case of a giant inguinoscrotal bladder hernia, which was solved by surgery. It includes a clinical, diagnostic and therapeutic aspects, and a review of the relative literature.

Hernia, Inguinal↗

[Metastatic hypernephroma of the stomach].

We report a case of renal cell adenocarcinoma (T2-G3) metastatic to the stomach in a patient who underwent a left radical nephrectomy and presented hematemesis and melena two weeks postoperatively. We were prompted to report this case because metastasis to the stomach is rare and the literature is scant. Despite treatment by radical surgery, the short disease-free period following nephrectomy, the high histological grade (G3) and the aggressive nature of the tumor have resulted in a short survival.

Carcinoma, Renal Cell↗

[Pleomorphic bladder rhabdomyosarcoma in an adult male. Apropos of a case].

We report on a 45-year-old male patient with a mesodermal tumor localized in the striated muscle of the bladder wall. The histopathologic analysis revealed a stage I pleomorphic tumor. The clinical and histologic features of this uncommon tumor type are described. Treatment by partial surgery and adjuvant chemo- and radiotherapy (CMT + XRT) have achieved good results. The patient is asymptomatic 44 months thereafter.

Combined Modality Therapy↗

[Sarcoma of the bladder. Report of 2 cases].

Discussion of a retrospective study in our unit of two cases of vesical tumours of mesenchymal origin, in adult patients and with different maturation behaviour. The first patient started with haematuria and after an extensive follow-up period is now free from the disease. The second patient was an accidental finding causing death in the course of the immediate postoperative.

Combined Modality Therapy↗

[Renal arteriovenous fistula, up-date and presentation of a new case].

Renal arteriovenous fistulae (AVF) conform a pathology the urologist is not used to see. The basic purpose of this paper is to collect and update the current knowledge of this renal-vascular disorder, quite frequently forgotten when establishing the likely causes of haematuria. The paper describes the etiology of renal AVF and their generation mechanisms, as well as clinical presentations they can have. A most appropriate diagnostic method is still selective renal arteriography, which usually evidences the anomaly through indirect arteriographic signs. However, when the lesion is small it can be difficult to detect it. Finally, a discussion of therapeutical possibilities, both conservative and radical, and a case recently treated in out unit are presented.

Aged↗

[Bladder metastasis of a renal cell carcinoma].

We report on a patient with renal adenocarcinoma that subsequently metastasized to the bladder. Although involvement of any organ in this area can lead to secondary invasion of the bladder wall, hematuria presenting in a patient previously submitted to nephrectomy due to hypernephroma should prompt us to strongly suspect tumor spread to the bladder. The forms of metastatic spread and treatment are discussed. Good results were achieved in our patient who, with a follow-up of 1.5 years, has had no tumor recurrence.

Carcinoma, Renal Cell↗

[Anderson-Hynes: results of the treatment of pyeloureteral junction syndrome].

This paper is a review of 63 cases of congenital Pyeloureteral Union Syndrome. A total of 47 patients were treated using the Anderson-Hynes reconstructive technique with 3-4 years follow-up. Incidence was analyzed by sex, age and side affected, without a clear predominance of one over the others being shown. Mean age at the time of diagnosis was 39-43 years. The predominant symptom is the presence of lumbo-abdominal pain (36.5%) but the lack of clinical symptoms is also frequent (25.3%). Pyelocalyceal lithiasis is the most frequent secondary pathology (28.5%). U.I.V. appears to be an irreplaceable means for diagnosis, achieving with this technique 93.6% of diagnosis. Hydronephrosis, in different degrees, and absence of ureteral contrast are the urographic signs most commonly found: 66% and 61% respectively. Using the Anderson-Hynes technique a rete of 85% good results can be obtained, with few complications and achieving disappearance of clinical symptoms and morphofunctional normality in a high percentage. Anderson-Hynes dismembered ureteropyeloplasty seems to be the choice technique for conservative surgical treatment of the P.U.U. syndrome.

Adolescent↗

[Hemospermia: clinical study].

We present a clinical study of 29 patients with macroscopic hemospermia. The associated symptoms prevailed over monosymptomatic presentation. Urethral-prostate-vesicular inflammation was the most common etiology (55%). We single out the presence of a seminal vesicle cyst, two malignant urogenital tumours and one patient with presentation of the post-radiotherapy symptom. In 24% of the cases the cause was unknown. Diagnosis was done preferably by means of case clinic and sexual history, physical exploration, prostate/seminal vesicle echography and bacteriological-cytological study of the urine fraction plus semen. We carried out other diagnostic explorations on a selective basis. We consider hemospermia to be a benign symptom, although its presence requires the carrying out of a methodical series of explorations to rule out other pathologies of very diverse condition worthy to being taken into account.

Adult↗

[Sarcomatoid carcinoma of the kidney: presentation of a case].

We describe a case of sarcomatoid variant, renal adenocarcinoma in a 69-year-old woman, whose death took place four months after the diagnosis was effected. We underline the form of clinical and radiological presentation, its low frequency, poor prognosis and difficult anatomopathological diagnosis.

Adenocarcinoma↗

[Bladder adenocarcinoma. Report of 2 new cases].

Another two cases of bladder adenocarcinoma (ADC), seen in 1988, are described herein. The most important aspects relative to tumor origin--urothelial and embryonal--are discussed. We review its clinical features and diagnosis, not unlike those of transitional cell tumors, although histologically different. We underscore the therapeutic aspects and poor prognosis in most of the cases.

Adenocarcinoma↗

[Castleman's disease, plasma-cellular variety: unusual finding in our specialty].

Castleman's disease is a disorder of the lymph tissue, of undetermined etiology and with preferentially mediastinal location, although other lymphatic and extra-lymphatic locations are also possible. This entry appears under two varieties: the most frequent, hyalovascular type which generally does not have associated systemic symptoms, and the plasmocellular type associated to multisystemic symptoms in up to 50% cases, such as fever, anaemia, hypergammaglobulinemia, etc. Additional examinations beyond those usually available are not enough to establish a certainty diagnosis against other types of tumours, so an histopathological study is required prior to arrive to this definite diagnosis. Surgery is the choice therapy, although sometimes a favourable response to radiotherapy, used as alternating or adjuvant therapy, can be obtained. Corticoid therapy can be an effective option when dealing with systemic symptoms. The paper submits one case of Castleman's disease of the hyalinovascular type with retroperitoneal location which forced us to establish a differential diagnosis with other disorders in that region more frequent in our specialty. Definite clinical diagnosis was not possible surgery was chosen and the entire lesion removed. As certainty diagnosis was therefore histologic and, up to this point, the patient has shown no signs or symptoms of relapsing.

Adult↗

[Renal adenocarcinoma in the isthmus of a horseshoe kidney].

A case of renal adenocarcinoma localized to the isthmus of a horseshoe kidney is described. We underscore the importance of complementary US and/or CT to urography to study the acquired pathologies of the horseshoe kidney because the pyelocaliceal distribution of these kidneys may not facilitate correct identification of certain space occupying lesions. The angiographic study is considered essential for planning surgery for this type of lesion.

Adenocarcinoma↗