Literature DB >> 16007610

Rhabdomyosarcoma arising within congenital cystic adenomatoid malformation.

Shyun Pai1, Hock-Liew Eng, Shin-Yi Lee, Chih-Cheng Hsiao, Wan-Ting Huang, Shun-Chen Huang.   

Abstract

Rhabdomyosarcoma arising within a congenital cystic adenomatoid malformation (CCAM) is an unusual entity. The patient underwent a lobectomy of his right lower lobe of lung due to a CCAM at the age of two. One year later, he developed a solid embryonal rhabdomyosarcoma at the same location. He received 1-year period chemotherapy and when the tumor reduced to a resectable size, surgical excision was done. The tumor cells appeared more differentiated after chemotherapy. The patient remains disease free to date, 16 months after surgery. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16007610     DOI: 10.1002/pbc.20481

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  3 in total

1.  FGF10 Signaling differences between type I pleuropulmonary blastoma and congenital cystic adenomatoid malformation.

Authors:  Guillaume Lezmi; Virginie Verkarre; Naziha Khen-Dunlop; Shamila Vibhushan; Alice Hadchouel; Caroline Rambaud; Marie-Christine Copin; Jean-Luc Rittie; Alexandra Benachi; Jean-Christophe Fournet; Christophe Delacourt
Journal:  Orphanet J Rare Dis       Date:  2013-09-03       Impact factor: 4.123

2.  Primary Pulmonary Alveolar Rhabdomyosarcoma in a Pediatric Patient: A Case Report With Literature Review.

Authors:  Bayan Hafiz; Hanaa Bamefleh
Journal:  Cureus       Date:  2022-01-15

3.  Cystic adenomatoid malformation in children: CT histopathological correlation.

Authors:  C Lanza; V Bolli; V Galeazzi; B Fabrizzi; G Fabrizzi
Journal:  Radiol Med       Date:  2007-06-11       Impact factor: 6.313

  3 in total

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