Primary Renal Rhabdomyosarcoma: An Unusual Bone Metastasizing Tumor of Kidney

被引:9
作者
Parvin, Shabnam [1 ]
Ghosh, Ranajoy [1 ]
Das, Ram Narayan [1 ]
Saha, Koushik [2 ]
Roy, Paromita [3 ]
Datta, Chhanda [1 ]
Chatterjee, Uttara [1 ]
机构
[1] Inst Post Grad Med Educ & Res, Dept Pathol, Kolkata, India
[2] NRS Med Coll, Dept Pediat Surg, Kolkata, India
[3] Tata Med Ctr, Dept Pathol, Kolkata, India
关键词
Renal neoplasm; rhabdomyosarcoma; undifferentiated sarcoma; OF-THE-LITERATURE; NEEDLE ASPIRATION BIOPSY; WILMS-TUMOR; PLEOMORPHIC RHABDOMYOSARCOMA; PREOPERATIVE CHEMOTHERAPY; CHILDHOOD; DIAGNOSIS; CHILDREN; SARCOMA; CANCER;
D O I
10.1080/15513815.2016.1175528
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Rhabdomyosarcoma (RMS) is one of the common malignant tumors in the pediatric age group. There is only a single case report of primary renal alveolar RMS. Fine needle aspiration (FNA) findings of primary renal RMS has not been reported so far. Hence we present an unusual case of primary alveolar RMS of the kidney. An 11 year old boy presented with an abdominal mass. On FNA a diagnosis of undifferentiated sarcoma and anaplastic Wilms tumor were considered. The tumor was resected and showed histopathological features of alveolar rhabdomyosarcoma. He developed multiple bony metastases and succumbed to the illness despite aggressive chemotherapy. RMS of the kidney should be considered in the differential diagnosis of children with a renal mass, and may have an aggressive clinical course with bone metastases.
引用
收藏
页码:251 / 259
页数:9
相关论文
共 29 条
[1]  
BRAY GL, 1986, AM J PEDIAT HEMATOL, V8, P75
[2]  
BRESLOW NE, 1986, CANCER-AM CANCER SOC, V58, P2501, DOI 10.1002/1097-0142(19861201)58:11<2501::AID-CNCR2820581125>3.0.CO
[3]  
2-V
[4]   Pleomorphic rhabdomyosarcoma in adults: A clinicopathologic study of 38 cases with emphasis on morphologic variants and recent skeletal muscle-specific markers [J].
Furlong, MA ;
Mentzel, T ;
Fanburg-Smith, JC .
MODERN PATHOLOGY, 2001, 14 (06) :595-603
[5]   UNRESECTABLE STAGE-IV NEPHROBLASTOMA - A POTENTIAL INDICATION FOR FINE-NEEDLE ASPIRATION BIOPSY IN CHILDREN [J].
GEISINGER, KR ;
WAKELY, PE ;
WOFFORD, MM .
DIAGNOSTIC CYTOPATHOLOGY, 1993, 9 (02) :197-201
[6]   Spindle cell sarcoma of the kidney with ganglionic elements (malignant ectomesenchymoma) associated with chromosomal abnormalities and a review of the literature [J].
Goldsby, RE ;
Bruggers, CS ;
Brothman, AR ;
Sorensen, PHB ;
Beckwith, JB ;
Pysher, TJ .
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1998, 20 (02) :160-164
[7]   Effect of duration of treatment on treatment outcome and cost of treatment for Wilms' tumor: A report from the National Wilms' Tumor Study group [J].
Green, DM ;
Breslow, NE ;
Beckwith, JB ;
Finklestein, JZ ;
Grundy, P ;
Thomas, PR ;
Kim, T ;
Shochat, S ;
Haase, G ;
Ritchey, M ;
Kelalis, P ;
D'Angio, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3744-3751
[8]  
GRIGNON DJ, 1988, CANCER-AM CANCER SOC, V62, P2027, DOI 10.1002/1097-0142(19881101)62:9<2027::AID-CNCR2820620926>3.0.CO
[9]  
2-6
[10]   Cellular Mesoblastic Nephroma in an Infant: Report of the Cytologic Diagnosis of a Rare Paediatric Renal Tumor [J].
Gupta, Ruchika ;
Mathur, Sandeep R. ;
Singh, Priti ;
Agarwala, Sandeep ;
Gupta, S. Datta .
DIAGNOSTIC CYTOPATHOLOGY, 2009, 37 (05) :377-380