گزارش موردی اکسترامدولاری پلاسماسیتومای بیضه
Authors
Abstract:
Extramedullary plasmacytomas are plasma cell tumors that arise outside the bone marrow. They are most often located in the head and neck. Extramedullary plasmacytomas account for approximately 3 percent of plasma cell malignancies. The diagnosis of an extramedullary plasmacytoma depends upon the demonstration of a monoclonal plasma cell tumor at an extramedullary site with no evidence of multiple myeloma based upon bone marrow examination and roentgenographic studies, absence of an M-protein in serum and/ or urine, and no related organ or tissue impairment. These tumors are highly responsive to local radiation therapy and rarely progress or recur. A 77 year old man referred for gradual enlargement of scrotum in April, 2004. He had no fever, weight loss or loss of appetite during the period. No tenderness, warmth or erythem of scrotum was observed on physical examination. No lymphadenopathy was detected. Later he had temporary relief because of antibiotic therapy . 7 months later, he referred again following the aggravation of his symptom. Ultrasonography of his scrotum was done and enlargement in the left testis was reported. Lab data including CBC,diff,ESR,AFP were normal but βHCG titer was reported higher than normal . He underwent radical orchiectomy and the specimen was sent for pathological study. Spermatocytic seminoma and plasmacytoma were suspected, but plasmacytoma was reported after the IHC . In order to rule out multiple myeloma, whole body bone scanning with sestamibi and urine Bence Jones protein were examined, all of which were negative. In bone marrow aspiration, the cellularity was normal and no pathologic lesion was reported. Considering clinical and paraclinical evidences, the diagnosis was extramedullary plasmacytoma.
similar resources
گزارش یک مورد پلاسماسیتومای اکسترامدولری حنجره
سابقه و هدف: پلاسماسیتوما در گروه سنی بالاتر از 25 سال، میزان بروز 30 در هر صدهزار نفر دارد. این نوع بیماری سه نوع تظاهر بالینی دارد. 1) میلوم مولتیپل 2) پلاسماسیتومای منفرد استخوانی 3) پلاسماسیتومای اکسترامدولری. در این مقاله به معرفی یک خانم مبتلا اقدام گردیده است. معرفی بیمار: بیمار خانم 57 ساله ای بود که یکسال قبل تشخیص میلوم مولتیپل برای ایشان داده شده بود علیرغم شیمی درمانی با دیسترس ...
full textگزارش یک مورد پلاسماسیتومای اکسترامدولری حنجره
سابقه و هدف: پلاسماسیتوما در گروه سنی بالاتر از 25 سال، میزان بروز 30 در هر صدهزار نفر دارد. این نوع بیماری سه نوع تظاهر بالینی دارد. 1) میلوم مولتیپل 2) پلاسماسیتومای منفرد استخوانی 3) پلاسماسیتومای اکسترامدولری. در این مقاله به معرفی یک خانم مبتلا اقدام گردیده است. معرفی بیمار: بیمار خانم 57 ساله ای بود که یکسال قبل تشخیص میلوم مولتیپل برای ایشان داده شده بود علیرغم شیمی درمانی با دیسترس تن...
full textگزارش یک مورد میکرولیتیازیس بیضه و کریپتورکدیسم
Testicular microlithiasis (TM) is an uncommon condition with reported prevalence of 0.6% in patients referred for scrotal ultrasound. Testicular microlithiasis was first reported by Priebe and Garret in 1970 and defined as multiple tiny calcification throughout the testis. The condition appears as characterstic small nonshadowing hyperechoic stippling foci in testicular parenchyma. Several as...
full textگزارش یک مورد سرطان بیضه فامیلیال
Testicular cancer allocate for only 1% of all male cancers, that 1-2% of them, would be familial. Family history of testicular cancer will be major risk factor. In this study, noticing the fact that familial testicular cancers are rare, we introduce cases of familiar testicular cancer. The first case was a 39-years-old man that came with abdominal enlargement, pain, and painless palpable masses...
full textMy Resources
Journal title
volume 14 issue 1
pages 73- 76
publication date 2006-04
By following a journal you will be notified via email when a new issue of this journal is published.
No Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023