Paternal behaviour in biparental hamsters, Phodopus campbelli, does not require contact with the pregnant female

2001 ◽  
Vol 62 (3) ◽  
pp. 453-464 ◽  
Author(s):  
Jennifer S. Jones ◽  
Katherine E. Wynne-Edwards
Animals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 718
Author(s):  
Gabriele Marino ◽  
Alessandra Sfacteria ◽  
Giuseppe Catone ◽  
Antonina Zanghì ◽  
Fabiana Pecchia ◽  
...  

Canine pseudo-placentational endometrial hyperplasia differs from the classical form of cystic endometrial hyperplasia for the well-organized tissue architecture resembling the canine placenta. After the discovery, it has been inconstantly reported. The present work reports the clinicopathological details of six spontaneous cases retrieved retrospectively from a large database. The lesion was found in young non-pregnant female dogs (median 2.0 years) at the end of dioestrus. It could be imaged by ultrasound and was always grossly detectable as single or multiple uterine enlargements of 2–3 cm in diameter with a villous whitish tissue growing on the mucosa and occluding the lumen. Histology confirmed the tissue architecture of the canine placenta with a basal glandular layer, a connective band, a spongy layer and a tortuous and compact labyrinth, often poorly recognizable. The pseudo-placentational hyperplasia is a non-inflammatory proliferative lesion although numerous mast cells inhabit the connective band, and a superimposed inflammatory infiltrate was seen in a case. Canine pseudo-placentational endometrial hyperplasia has very peculiar features, and it is a model for canine placentation and may help to better understand the cystic endometrial hyperplasia/pyometra complex.


2019 ◽  
Vol 8 (1) ◽  
Author(s):  
Khalid Farooqui ◽  
Hassan Abuzaid ◽  
Joyal Mathew ◽  
Farah Farooqui ◽  
Naseera Abubaker

2016 ◽  
Vol 48 (3) ◽  
pp. 264 ◽  
Author(s):  
Arham Shabbir ◽  
Sadia Shamsi ◽  
Muhammad Shahzad ◽  
HajraIkram Butt ◽  
Khurram Aamir ◽  
...  

2021 ◽  
Vol 8 (1) ◽  
pp. 1-3
Author(s):  
Farooq Ul Abidin ◽  

Foster Kennedy syndrome is a rare neurological entity that includes ipsilateral optic atrophy, contralateral papilledema, and sometimes anosmia. The syndrome has been described in association with a variety of intracranial pathologies such as a large frontal lobe tumor, olfactory groove meningioma, or medial third sphenoidal wing meningioma. In this report, we present a case of sphenoidal wing meningioma with Foster Kennedy syndrome in a 25-year-old pregnant female.


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