scholarly journals MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Elizabeth J. Perlman ◽  
Samantha Gadd ◽  
Stefan T. Arold ◽  
Anand Radhakrishnan ◽  
Daniela S. Gerhard ◽  
...  
Keyword(s):  
Favourable Histology

Didemnin B in favourable histology non-Hodgkin's lymphoma

1995 ◽  
Vol 13 (3) ◽  
pp. 257-260 ◽  
Author(s):  
G. Goss ◽  
A. Muldal ◽  
R. Lohmann ◽  
M. Taylor ◽  
P. Lopez ◽  
...  
Keyword(s):  
Hodgkin’S Lymphoma ◽  
Hodgkin's Lymphoma ◽  
Didemnin B ◽  
Favourable Histology ◽  
Non Hodgkin’S Lymphoma ◽  
Non Hodgkin's Lymphoma

Renal nephroblastoma in a 10-month-old boxer

2020 ◽  
Vol 8 (1) ◽  
pp. e001026
Author(s):  
Stephanie Richardson
Keyword(s):  
Survival Time ◽  
Clinical Signs ◽  
Abdominal Distension ◽  
Large Mass ◽  
Biochemical Profile ◽  
Wilms Tumour ◽  
Tumour Grading ◽  
Mean Survival Time ◽  
Favourable Histology ◽  
Space Occupying Lesion

A 10-month-old male entire Boxer dog was presented for weight loss and abdominal distension with a large mass palpable within the abdomen. A unilateral nephrectomy was performed for a large renal nephroblastoma (30-cm diameter). The nephroblastoma was suspected stage I, with favourable histology (human Wilms tumour grading). No adjunctive chemotherapy was administered. The dog remains clinically well 27 months postnephrectomy. Renal nephroblastomas are rare canine neoplasms and reported survival time is variable. This case and other recent reports suggest that mean survival time may be longer than previously thought. Nephroblastomas should be considered as a differential in young dogs presenting with clinical signs of an abdominal space-occupying lesion. The absence of azotaemia on a biochemical profile does not preclude significant renal pathology.

scholarly journals Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: A less complex karyotypic pattern?

1998 ◽  
Vol 79 (4) ◽  
pp. 361-364 ◽  
Author(s):  
Adewale Adeyinka ◽  
Fredrik Mertens ◽  
Ingrid Idvall ◽  
Lennart Bondeson ◽  
Christian Ingvar ◽  
...  
Keyword(s):  
Breast Carcinomas ◽  
Favourable Histology ◽  
Invasive Breast Carcinomas

scholarly journals Peripheral Neuroblastic Tumours

2019 ◽  
Vol 4 (02) ◽  
Author(s):  
Jasila Akbar ◽  
Prema Saldanha
Keyword(s):  
Retrospective Study ◽  
Adrenal Gland ◽  
Neural Crest ◽  
Nervous Tissue ◽  
Age Group ◽  
Favourable Histology ◽  
Pathology Classification ◽  
Microscopic Features ◽  
Neuroblastic Tumour ◽  
Sympathetic Nervous

Background: Peripheral neuroblastic tumours arise from the neural crest cells in the sympathetic nervous tissue. These are rare, but are the most common among the extracranial solid tumours occurring in children. Method: This was a retrospective study conducted on 15 cases of peripheral neuroblastic tumours. The demographic details were recorded and the slides were analysed for the microscopic features and classified according to International Neuroblastoma Pathology Classification (INPC). Results: Out of the 15 peripheral neuroblastic tumour cases, 8 were males and 7 females. Seven cases came under age group <1.5years, 5 were between 1.5 years to 5 years and 5 cases were over 5 years of age. Seven tumours were from the retroperitoneal region, 4 cases were from the adrenal gland, 2 from intracranium and one case each was from the neck and the mediastinal regions. There were 8 Neuroblastoma cases, 2 cases of Ganglioneuroblastoma and 5 cases of Ganglioneuroma. It was found that 8 tumours were in the favourable histology group and 7 tumours in the unfavourable histology group. Conclusion: Peripheral neuroblastic tumours are rare. It is important to classify them accurately according to the various categories which help to determine the prognosis.

Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse

2006 ◽  
Vol 210 (1) ◽  
pp. 49-58 ◽  
Author(s):  
R Natrajan ◽  
RD Williams ◽  
SN Hing ◽  
A Mackay ◽  
JS Reis-Filho ◽  
...  
Keyword(s):  
Array Cgh ◽  
Favourable Histology ◽  
Gains And Losses

P43: Genomic changes in favourable histology Wilms tumours analysed by genome-wide 1 Mb-spaced and chromosome 1 tiling-path array CGH

2005 ◽  
Vol 48 (4) ◽  
pp. 507-508
Author(s):  
Rachael Natrajan ◽  
Richard Williams ◽  
Sandra Hing ◽  
Suzanne Little ◽  
Alan Mackay ◽  
...  
Keyword(s):  
Array Cgh ◽  
Chromosome 1 ◽  
Genomic Changes ◽  
Favourable Histology ◽  
Genome Wide
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