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1.
Int Urol Nephrol ; 55(3): 589-596, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36454449

ABSTRACT

PURPOSE: This study was done to find out the clinicopathological characteristics of carcinoma penis in Nepali population and to evaluate various risk factors that predict its inguinal lymph node metastasis. METHODS: A retrospective cross-sectional study was carried out at the Urology Unit, Department of Surgical Oncology at BP Koirala Memorial Cancer Hospital, Bharatpur, Nepal. Case notes of biopsy-proven penile cancer, from January 2012 to December 2021, who underwent some form of surgical intervention were included. RESULTS: A total of 380 patients were included in the study. The mean age of the patients was 55.92 ± 13.81 years. At presentation, 78.5% had clinically node-positive disease. The most common treatment for the primary tumor was partial amputation of the penis (74.2%). Bilateral inguinal lymph node dissections were done in 370 cases. The most common histology was the usual SCC in 94.2% of cases and 69% were well differentiated. T3 was the most common staging in 49.4% cases. Pathologically nodal negative status was found in 58% cases. In univariate analysis, factors like duration of symptoms (≥ 6 months), high-risk histopathology (basaloid/sarcomatoid variant), increased T-stage, poorly differentiated tumor, and the presence of PNI or LVI were significantly associated with lymph node metastasis. CONCLUSIONS: Penile cancer is a common cancer in developing countries such as Nepal. The majority of the patients present late. Early recognition and prompt treatment are required to improve the overall outcome.


Subject(s)
Carcinoma, Squamous Cell , Penile Neoplasms , Male , Humans , Adult , Middle Aged , Aged , Lymphatic Metastasis , Retrospective Studies , Carcinoma, Squamous Cell/pathology , Penile Neoplasms/pathology , Nepal , Cross-Sectional Studies , Lymph Node Excision , Sentinel Lymph Node Biopsy , Penis/pathology , Neoplasm Staging
2.
JNMA J Nepal Med Assoc ; 52(190): 388-90, 2013.
Article in English | MEDLINE | ID: mdl-24362666

ABSTRACT

A solitary fibrous tumour is an unusual spindle cell neoplasm. It frequently arises from the serosal surface of pleural cavity but has recently been described in diverse extrapleural sites. Urogenital localization is rare and only 36 cases of solitary fibrous tumours of the kidney have been described on published report. We report a case of a large solitary fibrous tumour clinically and radiologically thought to be renal cell carcinoma arising in the kidney of a 30 year old female. The radical nephrectomy was performed. The tumour was a well- circumscribed, solid mass attached to the renal pelvis without necrosis and haemorrhage. Histopathologically, a spindle cell neoplasia with alternating hypo and hypercellular areas, storiform, fascicular and hemangipericytoma like growth pattern and less cellular dense collagen deposits were observed. Immunohistochemical studies revealed reactivity for CD34, CD99 and Bcl-2 protein.


Subject(s)
Kidney Neoplasms/diagnosis , Solitary Fibrous Tumors/diagnosis , Adult , Carcinoma, Renal Cell/diagnosis , Female , Humans , Immunohistochemistry , Kidney Neoplasms/metabolism , Kidney Neoplasms/pathology , Kidney Neoplasms/surgery , Nephrectomy , Solitary Fibrous Tumors/metabolism , Solitary Fibrous Tumors/pathology , Solitary Fibrous Tumors/surgery
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