scholarly journals Paroxysmal cold hemoglobinuria in a 7-year-old male child – Was it really cold induced? A diagnostic and management dilemma

Author(s):  
Akash Kumar ◽  
Siyaram Didel ◽  
Daisy Khera ◽  
Anubhav Gupta ◽  
Abhishek Purohit
1978 ◽  
Vol 48 (4) ◽  
pp. 452-453
Author(s):  
WILLIAM BURNETT ◽  
BRIAN DOUGLAS ◽  
KEVIN DWYER ◽  
COLIN KENNARD ◽  
GARY ROBERTS

2017 ◽  
Vol 20 (4) ◽  
pp. 335-339 ◽  
Author(s):  
Brent R Weil ◽  
Alyaa Al-Ibraheemi ◽  
Sara O Vargas ◽  
Shawn J Rangel

Autoamputation of the appendix has previously been reported in the literature, but it is likely an unusual event. We report a 2-year-old male child who had previously undergone laparotomy and bowel resection for necrotizing enterocolitis. Two years later a calcified intra-abdominal mass was identified on abdominal radiography and ultrasonography. Eventual laparotomy revealed a densely calcified mass within the transverse mesocolon. The mass was uneventfully resected. Pathologic evaluation showed appendiceal tissue, consistent with prior autoamputation of the vermiform appendix. Autoamputation of the appendix has not to our knowledge previously been associated with a calcified mass nor been associated with a history of necrotizing enterocolitis, and these factors distinguish this case as noteworthy.


1969 ◽  
Vol 62 (5) ◽  
pp. 513
Author(s):  
HOWARD M. RADWIN
Keyword(s):  

PEDIATRICS ◽  
2014 ◽  
Vol 134 (1) ◽  
pp. e284-e288 ◽  
Author(s):  
D. Grieb ◽  
A. Feldkamp ◽  
T. Lang ◽  
M. Melter ◽  
C. Stroszczynski ◽  
...  

1996 ◽  
Vol 45 (1-2) ◽  
pp. 255-261 ◽  
Author(s):  
S. Ramsden ◽  
L. Gaunt ◽  
A. Seres-Santamaria ◽  
J. Clayton-Smith

AbstractA male child has been identified with Angelman syndrome. He has been shown to carry a de novo Robertsonian 15/15 translocation where both chromosome 15s have been derived from the father. Consequently the disease in this instance is due to paternal uniparental disomy.


2016 ◽  
Vol 33 (4) ◽  
pp. 467-469 ◽  
Author(s):  
Metin Uysalol ◽  
Gunes Parlakgul ◽  
Yasin Yilmaz ◽  
Agop Cİtak ◽  
Nedret Uzel
Keyword(s):  

2017 ◽  
Vol 06 (02) ◽  
pp. 122-125
Author(s):  
Saurabh Verma ◽  
M. Sridhar ◽  
S. Shashivadhanan ◽  
Manish Garg

AbstractIt is a rare and underdiagnosed entity. The adagium “one only sees what one knows” is certainly true in cases of Blake's pouch cyst, as all types of posterior fossa cysts and cyst-like malformations may present nearly identical on initial imaging studies. Only one case of Blake's pouch cyst has been reported from this country, except for a case in utero, in which a diagnosis of Blake's pouch cyst was made on prenatal ultrasound and later confirmed by MRI. In this report we describe a case of Blake's pouch cyst in a 9-month-old male child along with the principles of diagnosis of Blake's pouch cyst, in combination with literature review. Differentiating Blake's pouch cyst from other posterior fossa cysts and cyst-like malformations and recognizing the accompanying hydrocephalus that are essentially noncommunicating have important implications not only on clinical management but also on genetic counseling, which is unnecessary in case of Blake's pouch cyst.


2009 ◽  
Vol 14 (26) ◽  
pp. 46 ◽  
Author(s):  
Tânia Mara Campos de Almeida ◽  
Maria Aparecida Penso ◽  
Liana Fortunato Costa

Sign in / Sign up

Export Citation Format

Share Document