favourable histology
Recently Published Documents


TOTAL DOCUMENTS

10
(FIVE YEARS 2)

H-INDEX

4
(FIVE YEARS 0)

2020 ◽  
Vol 8 (1) ◽  
pp. e001026
Author(s):  
Stephanie Richardson

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.


Author(s):  
Jasila Akbar ◽  
Prema Saldanha

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.


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

2006 ◽  
Vol 210 (1) ◽  
pp. 49-58 ◽  
Author(s):  
R Natrajan ◽  
RD Williams ◽  
SN Hing ◽  
A Mackay ◽  
JS Reis-Filho ◽  
...  

2005 ◽  
Vol 48 (4) ◽  
pp. 507-508
Author(s):  
Rachael Natrajan ◽  
Richard Williams ◽  
Sandra Hing ◽  
Suzanne Little ◽  
Alan Mackay ◽  
...  

Author(s):  
Adewale Adeyinka ◽  
Fredrik Mertens ◽  
Ingrid Idvall ◽  
Lennart Bondeson ◽  
Christian Ingvar ◽  
...  

1995 ◽  
Vol 13 (3) ◽  
pp. 257-260 ◽  
Author(s):  
G. Goss ◽  
A. Muldal ◽  
R. Lohmann ◽  
M. Taylor ◽  
P. Lopez ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document