Perinatal pubic symphysis separation combined with pubic fracture: a case report and literature review

Author(s):  
Liang Deng ◽  
Liang-Yu Xiong ◽  
Ji-Huan Zeng ◽  
Qiang Xiao ◽  
Yuan-Huan Xiong
2015 ◽  
Vol 14 (2) ◽  
pp. 105-110
Author(s):  
Valentinas Uvarovas ◽  
Povilas Žukauskas ◽  
Tadas Šiatkus ◽  
Povilas Masionis

Postpartum diastasis of the pubic symphysis has the incidence from 1 in 300 to 1 in 30,000 deliveries. Under the action of progesterone and relaxin, a 1 cm widening of pubic symphysis is considered to be physiological and necessary for normal delivery. However, any higher widening is always pathological, involving the damage of pubic and sacroiliac ligaments. Multiparity has been identified as the only independent risk factor. Because this pathology often manifests as chronic pain in the pubic symphysis region, it is often mistakenly stated as a normal postpartum occurrence. It is only later when the symptoms of pelvic instability and pubic osteitis appear. Postpartum symphysiolysis is a clinical challenge to a physician due to low awareness and the postpartum period important to both the patient and the newborn.


2013 ◽  
Vol 2013 ◽  
pp. 1-4 ◽  
Author(s):  
Pande Made Wisnu Tirtayasa ◽  
Robertus Bebet Prasetyo ◽  
Arry Rodjani

Diphallia or penile duplication is an extremely rare congenital anomaly. It occurs once in every 5.5 million live births. The extent of penile duplication and the number of associated anomalies vary greatly, ranging from a double glans from a penis with no associated anomaly up to complete penile duplication associated with multiple anomalies. Here, we report a 12-year-old boy with complete bifid diphallia associated with bifid scrotum, epispadia, and pubic symphysis diastasis along with a review of the articles pertaining to this anomaly.


2009 ◽  
Author(s):  
C. L. Khoo ◽  
L. Regina ◽  
S. R. K. Naik ◽  
S. Kang

2017 ◽  
Author(s):  
T Stopp ◽  
M Feichtinger ◽  
W Eppel ◽  
T Stulnig ◽  
P Husslein ◽  
...  

1998 ◽  
Vol 37 (04) ◽  
pp. 141-145
Author(s):  
F. J. C. Pallarés ◽  
A. R. Bartual ◽  
Susana Tenes Rodrigo ◽  
F. J. Ampudia-Blasco ◽  
C. R. de Ávila y Ávalos ◽  
...  

SummaryA case of a 49-year-old man suffering from bilateral adrenocortical carcinoma with local and secondary rapid progression is reported. The results of adrenocortical scintigraphy (NP 59) and histological findings allowed the diagnosis. This case report and a literature review showed the importance of using adrenocortical scintigraphy as a complementary imaging procedure of CT or MR images.


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