Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ala B. Hamoudi"'
Autor:
Stephen J. Qualman, Harold M. Maurer, Ala B. Hamoudi, Bruce R. Pawel, Lina Asmar, Bruce Webber, William A. Newton, Frederick B. Ruymann
Publikováno v:
Medical and Pediatric Oncology. 29:170-180
Undifferentiated soft tissue sarcoma (UND-STS) is the most poorly defined tumor eligible for intergroup Rhabdomyosarcoma Studies (IRS). Recent IRS UND-STS experience was reviewed to assess the histologic characteristics and clinical behavior of undif
Autor:
Harold M. Maurer, William A. Newton, Ala B. Hamoudi, Roman Kodet, Moody D. Wharam, Lina Asmar
Publikováno v:
Medical and Pediatric Oncology. 29:51-60
Children and adolescents who develop rhabdomyosarcoma (RMS) and related sarcomas in the orbit and treated on Intergroup Rhabdomyosarcoma protocols have had an extremely high cure rate. This study evaluates the possible relationship between their tumo
Autor:
Sayuri Suzuki, Stephen J. Qualman, Ala B. Hamoudi, William A. Newton, Hiroshi Hojo, Haruki Wakasa, Florinda Jaynes
Publikováno v:
The American Journal of Surgical Pathology. 19:1224-1236
Pseudosarcomatous myofibroblastic tumor (PMT) is the result of reactive proliferation of myofibroblasts. In children, PMT of the urinary bladder can be mistaken for embryonal rhabdomyosarcoma clinically, radiologically, and by light microscopy. We ar
Autor:
David M. Parham, Frank Gonzalez-Crussi, Dieter Harms, Andrea O. Cavazzana, Timothy J. Triche, Harold M. Maurer, Henry B. Marsden, Bruce L Webber, Hiroyuki Shimada, Vito Ninfo, Lina Asmar, A. J. M. van Unnik, William A. Newton, Dietmar Schmidt, Maria C. Tsokos, Herbert M. Reiman, Nancy E. Sachs, Mohan Beltangady, Ala B. Hamoudi, Edmund A. Gehan
Publikováno v:
Cancer. 76:1073-1085
Background. There is a need to develop a single prognostically significant classification of rhabdomyosarcomas (RMS) and other related tumors of children, adolescents, and young adults which would be a current guide for their diagnosis, allow valid c
Autor:
Richard S. Pieters, Ala B. Hamoudi, Thomas A. Olson, Edward J. Kosnik, Frederick B. Ruymann, Kathryn J. Klopfenstein, Emel Bayar
Publikováno v:
Journal of Pediatric Hematology/Oncology. 17:71-75
Malignant rhabdoid tumor (MRT) of the central nervous system (CNS) is pathologically identical to MRT of the kidney. CNS MRTs have the clinicopathological behavior of a high-grade intracranial sarcoma, and the children have a very poor prognosis. We
Autor:
Andrea O. Cavazzana, Adrian J. M. Van Unnik, Mohan S. Beltangady, Dieter Harms, Dietmar Schmidt, William A. Newton, Ala B. Hamoudi, Edmund A. Gehan, Herbert M. Reiman, Frank Gonzales-Crussi, Hiroyuki Shimada, Henry B Marsden, Vito Ninfo, Timothy J. Triche, Maria Tsokos, Harold M. Maurer, David M. Parham, Lina Asmar, Bruce Webber, Nancy Sachs
Publikováno v:
Cancer. 74:2579-2588
Background. An International Pathology study was conducted to measure the agreement demonstrated among and within groups of pathologists involved in the categorization of childhood rhabdomyosarcoma according to four pathology classifications. Data co
Autor:
Nancy Sachs, Dietmar Schmidt, Ala B. Hamoudi, Lina Asmar, H. M. Maurer, Dieter Harms, William A. Newton, Ivo Leuschner
Publikováno v:
The American Journal of Surgical Pathology. 17:221-230
We reviewed 173 cases of paratesticular rhabdomyosarcoma (RMS) of Intergroup Rhabdomyosarcoma Studies (IRS)-I, -II, and -III for evaluation of possible histological factors that might account for the good prognosis of these patients. Almost all cases
Autor:
Ala B. Hamoudi, Stephen J. Qualman
Publikováno v:
Pediatric Pathology. 12:263-267
Publikováno v:
The American Journal of Surgical Pathology. 15:257-267
A group of 27 rhabdomyosarcomas (RMS) whose histology showed abundant cells containing cytoplasmic intermediate-filament globular inclusions resembling those seen in rhabdoid tumors has been identified among Inter-group Rhabdomyosarcoma Study (IRS) I
Publikováno v:
Medical and Pediatric Oncology. 18:110-118
Liver biopsies were done on 20 patients with histiocytosis X (HX) as part of pretreatment evaluation prior to entry on two Childrens Cancer Study Group protocols. Seventeen patients had hepatomegaly, and seven had one or more abnormal laboratory para