Subject(s)
Papillomavirus Infections , Urethritis/virology , Alphapapillomavirus/classification , Alphapapillomavirus/isolation & purification , Alphapapillomavirus/pathogenicity , Combined Modality Therapy , Condylomata Acuminata/diagnosis , Condylomata Acuminata/drug therapy , Condylomata Acuminata/epidemiology , Condylomata Acuminata/prevention & control , Condylomata Acuminata/surgery , Condylomata Acuminata/virology , Female , Genital Diseases, Female/diagnosis , Genital Diseases, Female/drug therapy , Genital Diseases, Female/epidemiology , Genital Diseases, Female/prevention & control , Genital Diseases, Female/surgery , Genital Diseases, Female/virology , Genital Diseases, Male/diagnosis , Genital Diseases, Male/drug therapy , Genital Diseases, Male/epidemiology , Genital Diseases, Male/prevention & control , Genital Diseases, Male/surgery , Genital Diseases, Male/virology , Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 , Humans , Male , Papillomavirus Infections/drug therapy , Papillomavirus Infections/epidemiology , Papillomavirus Infections/prevention & control , Papillomavirus Infections/transmission , Papillomavirus Vaccines , Urethritis/diagnosis , Urethritis/epidemiology , UrologyABSTRACT
No disponible
No disponible
Subject(s)
Humans , Male , Urology , Tumor Virus Infections/epidemiology , Condylomata Acuminata/epidemiology , Condylomata Acuminata/prevention & control , Urologic Diseases/epidemiology , Urologic Diseases/prevention & control , Urological ManifestationsABSTRACT
No disponible
Subject(s)
Humans , Male , Middle Aged , Neoplasm Metastasis/diagnosis , Neoplasm Metastasis/pathology , Neoplasm Metastasis , Alkaline Phosphatase/therapeutic use , Low Back Pain/complications , Prostate/pathology , Prostate/surgery , Prostate , Prostatic Neoplasms/therapy , Testosterone/therapeutic useABSTRACT
A rare case of asymtomatic synchronous bilateral granulomatous orchitis idiopathic is decribed. In the scrotal ultrasonography are multiple hypoecoic areas, differential diagnosis between testicular tumor and granulomatous orchitis is very difficult in any examination by histological findings.
Subject(s)
Orchitis/diagnosis , Aged , Granuloma/pathology , Humans , MaleABSTRACT
Describimos un raro caso de sincronismo asintomático de orquitis idiopática granulomatosa bilateral. La ecografia escrotal muestra múltiples áreas hipocóicas, el diagnóstico diferencial entre tumor y orquitis granulomatosa es muy difícil y sólo el examen histológico lo confirmará (AU)
A rare case of asymtomatic synchronous bilateral granulomatous orchitis idiopathic is decribed. In the scrotal ultrasonography are multiple hypoecoic areas, differential diagnosis between testicular tumor and granulomatous orchitis is very difficult in any examination by histological findings (AU)
Subject(s)
Humans , Male , Aged , Orchitis/diagnosis , Orchiectomy , Neoplasms, Multiple Primary/diagnosis , Diagnosis, Differential , Biomarkers, Tumor/analysisSubject(s)
Pain , Testicular Diseases , Chronic Disease , Humans , Male , Pain/etiology , Pain Management , Testicular Diseases/etiology , Testicular Diseases/therapyABSTRACT
No disponible
Subject(s)
Male , Humans , Testicular Diseases/diagnosis , Pain/etiology , Analgesics/therapeutic useABSTRACT
Spermatic cord sarcomas are rare tumours. Dedifferentiated liposarcoma accounts for only 10% of all spermatic cord sarcomas. These are usually large-sized tumours histologically characterised for being well-differentiated liposarcomas with some high grade sarcoma areas. Volume, location, mass homogeneity as well as presence of pelvic and retroperitoneal adenopathies are reported by CT and ultrasound techniques. These are useful for post-treatment follow-up. This paper presents one spermatic cord, dedifferentiated liposarcoma from which lipomas from the same spermatic cord had been previously removed in three occasions. We believe this is a degeneration of the earlier resected lipoma. Management is by extended inguinal radical orchiectomy. Value of adjuvant radio- and chemotherapy is uncertain. Post-surgery local relapses are common, and haematogenous and pelvic nodes metastasis likely. Survival at 5 and 10 years is 75% and 63% respectively.
Subject(s)
Genital Neoplasms, Male/pathology , Lipoma/pathology , Liposarcoma/pathology , Spermatic Cord/pathology , Genital Neoplasms, Male/complications , Genital Neoplasms, Male/surgery , Humans , Lipoma/complications , Lipoma/surgery , Liposarcoma/complications , Liposarcoma/surgery , Male , Middle Aged , Spermatic Cord/diagnostic imaging , Spermatic Cord/surgery , Tomography, X-Ray Computed , Treatment OutcomeSubject(s)
Lichen Sclerosus et Atrophicus/pathology , Penile Diseases/pathology , Precancerous Conditions/pathology , Adult , Balanitis/complications , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/pathology , Follow-Up Studies , Humans , Hyperplasia , Lichen Sclerosus et Atrophicus/epidemiology , Male , Middle Aged , Penile Diseases/epidemiology , Penile Neoplasms/epidemiology , Penile Neoplasms/pathology , Precancerous Conditions/epidemiologyABSTRACT
Los sarcomas del cordón espermático son tumores de rara presentación. El liposarcoma dediferenciado representa sólo un 10 por ciento de los sarcomas del cordón espermático. Estos suelen ser tumores de gran tamaño y con una histología caracterizada por ser un liposarcoma bien diferenciado con áreas de sarcoma de alto grado. El TAC y la ecografía nos informarán del volumen, localización, homogeneidad de la masa, así como de las posibles adenopatías pelvianas y retroperitoneales. Son útiles en el seguimiento después del tratamiento. Nosotros presentamos un liposarcoma dediferenciado, de cordón espermático, al que previamente, se le extirpó en tres ocasiones lipomas en el mismo cordón espermático. Creemos que se trata de una degeneración del lipoma previo resecado. El tratamiento es la orquiectomía radical por vía inguinal amplia, siendo la radioterapia y la quimioterapia de ayuda complementaria, con valor incierto. Suelen presentar recidivas locales frecuentes después de la cirugía, pudiendo presentar metástasis hematógenas y en nódulos pelvianos. Presentan una supervivencia a los 5 y 10 años, de un 75 por ciento y 63 por ciento respectivamente (AU)
Subject(s)
Middle Aged , Male , Humans , Spermatic Cord , Tomography, X-Ray Computed , Treatment Outcome , Lipoma , Liposarcoma , Genital Neoplasms, MaleABSTRACT
No disponible
Subject(s)
Middle Aged , Adult , Male , Humans , Lichen Sclerosus et Atrophicus , Penile Diseases , Precancerous Conditions , Balanitis , Carcinoma, Squamous Cell , Hyperplasia , Follow-Up Studies , Penile NeoplasmsABSTRACT
Presentamos un caso de cistoadenoma papilar de epidídimo, tumor epitelial benigno muy poco frecuente. Relacionado con la enfermedad de von Hippel-Lindau, puede estar asociado a infertilidad. Se suele presentar en el adulto joven, en un tercio estas lesiones son bilaterales, diagnosticándose por palpación y sobre todo por la ecografía. El tratamiento es la exéresis quirúrgica y posterior seguimiento de cerca. Está descrita la transformación en 2 casos de cistoadenoma de epidídimo en cistoadeno-carcinoma (AU)
Subject(s)
Adult , Male , Humans , Epididymis , Cystadenoma, Papillary , Testicular NeoplasmsABSTRACT
Contribution of one case report of papillary cystadenoma, a very uncommon benign epithelial tumour. Related to von Hippel-Lindau's disease, it may be associated to infertility. It tends to occur in young adults, lesions being bilateral in one third of cases. It is diagnosed through palpation and particularly with ultrasound techniques. Management is via surgical exeresis and subsequent watchful follow-up. Two cases reported transformation of epididymis cystadenoma to cystadenocarcinoma.
Subject(s)
Cystadenoma, Papillary/pathology , Epididymis , Testicular Neoplasms/pathology , Adult , Humans , MaleABSTRACT
In spite of being the most frequent tumour in this location, together with adenomatoid tumours, the spermatic cord lipoma is a very rare entity (30-35% each). The etiology is unknown but linked to a constitutional factors, obesity, an its presentation is more frequent in the fifth or sixth decade of life. It progresses always as an asymptomatic tumour, usually unilateral, showing a swift growth to masses larger than 10 cm. Diagnosis is reached by ultrasound and CAT when doubtful, and the histology is confirmed during scrotomy. Tumour resection is the choice treatment. In the case reported here there had been two earlier resections, so relapses and pseudo-relapses should be taken into account. Although rare, a few cases of lipoma degeneration to liposarcoma have been reported.
