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1.
Pakistan Journal of Medical Sciences. 2011; 27 (1): 212-213
in English | IMEMR | ID: emr-112908

ABSTRACT

Metastatic paranasal sinuses and orbital cancer is very rare. The patient with sinusitis and orbital symptoms warrants a detailed history, complete physical examination and serial radiological tests [sinus radiographs and CT scan] to rule out any metastatic disease and prompt treatment. We present a case of 65 years old patient with metastatic prostate cancer who presented to us with left ethmoid sinuses and orbital metastasis causing ipsilateral proptosis


Subject(s)
Humans , Male , Orbital Neoplasms/pathology , Ethmoid Sinus , Neoplasm Metastasis , Exophthalmos , Prostatic Neoplasms/secondary , Paranasal Sinus Neoplasms/diagnostic imaging , Biopsy
2.
Urology Annals. 2011; 3 (2): 103-107
in English | IMEMR | ID: emr-124068

ABSTRACT

Peripheral primitive neuroectodermal tumor/Ewing's sarcoma [PNET/EWS] is primarily a tumor of soft tissues and bones. Primary localization of PNET/EWS in genitourinary organs is rare. No data on this localization of PNET/EWS are available in literature from Pakistan. We searched our adult uro-oncology records from 1994 till date and identified all cases of adult genitourinary and adrenal PNET/EWS diagnosed on histology and immunohistochemistry. Their case records were reviewed to obtain data on demographics, presentation, pathologic features, management and outcome. Six cases were found; all were young and had aggressive disease at presentation. Four had renal PNET/EWS. One case each of prostate and adrenal PNET/EWS was seen. Surgery and chemotherapy formed the mainstay of management. Three patients [50%] died during treatment, two were lost to follow-up and one case with renal PNET/EWS showed good initial response to chemotherapy but was later on lost to follow-up. In conclusion, PNET/EWS should be considered in the differential diagnosis of genitourinary malignant tumors in young patients. These tumors are aggressive with poor outcome


Subject(s)
Humans , Female , Male , Kidney Neoplasms , Nephrectomy , Adrenal Gland Neoplasms , Sarcoma, Ewing , Urologic Neoplasms
3.
Professional Medical Journal-Quarterly [The]. 2011; 18 (3): 344-349
in English | IMEMR | ID: emr-113342

ABSTRACT

Hereditary nonpolyposis colorectal cancer [HNPCC] is the most common form of hereditary bowel cancer. Multiple generations are affected with colorectal cancer at relatively young age, between 25 and 45 years. To investigate the frequency of HNPCC in Pakistani population, due to the high incidence of colorectal cancer in younger Pakistani adults and prevalence of consanguinity in this region conducted this study. November 2008 and January 2010. Ninty histopathologically confirmed colorectal cancer patients between 12- 50 years and their families were interviewed using a detailed questionaire. The questions about family history of colorectal cancer, history of other cancers, age at diagnosis and consanguinity were asked. The pedigrees were drawn for all families based on given information. Hospital records were also reviewed to confirm cancers reported in relatives. Amsterdam criteria was used to label a family as HNPCC. Seventeen patients [18.9%] had one or more first or second degree relatives under age 50 years with colorectal cancers suggestive of HNPCC. Another 15 patients [16.7%] had first or second degree relatives with a family history of other extra-colonic cancers including ovarian, breast, endometrium, lung, parotid, brain and bladder cancer. Of these 30 patients [33.3%] reported that their parents were first degree cousins. 1. High frequency of HNPCC is seen in Pakistani population. 2. Higher proportion of colorectal cancer is seen in young Pakistanis. Strong prevalence of consanguineous marriages could be important factors for HNPCC occurrence in Pakistan. Future studies with large sample size along with genetic testing and screening programmes are warranted

4.
Pakistan Journal of Medical Sciences. 2011; 27 (4): 806-811
in English | IMEMR | ID: emr-113665

ABSTRACT

We evaluated the treatment outcome and associated prognostic factors for patients with nonseminomatous testicular germ cell tumours [NSGCT], who were treated in our hospital during last 15 years. Data was retrospectively analyzed for the 1995 through 2010 period. One hundred and twenty patients with NSGCT were identified. Descriptive Data was analyzed for the age, risk factors, site, histology, stage, chemotherapy regimen, retroperitoneal lymph node dissection [RPLND] and radiological response. The disease free survival [DFS] and overall survival [OS] were determined by Kaplan and Meier method and statistical inferences with the log-rank test. Cox proportional hazards Model was used to find different prognostic factors. Mean age of patients was 29.65 years [16-45]. Pain and swelling of testis was commonest presentation [30%]. Right sided were predominant [63.3%]. Predominant stage was IIIC [55%] and commonest histology was mixed [embryonal cell carcinoma+yolk sac tumor+teratoma] in 45% cases. Majority of patients were poor risk according to International Germ Cell Cancer Consensus Classification [IGCCC], 41.7%. Bleomycin, etoposide and cisplatinum [BEP] chemotherapy was mostly as a first line treatment [87.5%]. Postchemotherapy RPLND was performed in 31 patients [25.8%]. Histology among residuals was fibrosis [48.4%], viable tumors [35.5%] and mature teratoma [16.1%]. Median DFS and OS were 9 and 9.1 years respectively. Stage, IGCCC, RPLND were found important prognostic factors [p < 0.001]. Better outcome with lower disease burden and lower IGCCC and multidiscplinary approach warrants public awareness should be carried out for the testicular self-examination to reduce the time from the beginning of symptoms to time of seeking treatment

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