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1.
Maroc Medical. 2003; 25 (1): 17-21
in French | IMEMR | ID: emr-63434
2.
Maroc Medical. 2002; 24 (3): 164-8
in French | IMEMR | ID: emr-60025

ABSTRACT

We report here a study of 7 cases of thyroid cancer in childhood. This study that we reinforced by literature review aims to point out the different aspects of this affection: clinical features, the complementary examinations and the management to diagnoses it with certainty and lastly, the different therapeutical attitudes. It is a study of 7 children between 8 and 15 years aged, with a female daminance, without pearicular previous medical histories. Clinically, these children present an euthyroidal goitre, cervical adenopathies with conservation of good general health condition. Scintigraphy showed a cold nodule that was proved to be neoplastic at the anatomo-pathological study, it was papillar or papillo-vesicular carcinoma. The surgical management has at the present time a tendancy to conservative surgery combined or not with a ganglionic curage, followed by a substitute hormonal treatment. In general, the prognosis of this affection is good for the differentiated forms whereas it remains has for bad anaplastic non differentiated forms


Subject(s)
Humans , Male , Female , Child , Thyroid Neoplasms/diagnosis , /therapy
3.
Maroc Medical. 2002; 24 (4): 262-266
in French | IMEMR | ID: emr-60040

ABSTRACT

Currarino's triad is a congenital malformation involving the combination of anorectal stenosis, a presacral mass and an anterior sacral bony defect. A new case is reported in a male neonate, who developed intestinal obstruction on the second day of life. The examination revealed a high anorectal malformation. A colostomy was performed. Partial agenesis of the sacrum was diagnosed radiologically. Computed tomographic myelography demonstated an anterior sacral meningocele and a tethered spinal cord. Excision of the meningocele and untethering of a tethered spinal cord were performed. Secondly, posterior sagittal anorectoplasty was performed. Colostomy was closed 3 months after rectal dilatations. Early diagnosis and management is recommended to avoid the high mortality and morbidity associated with this condition


Subject(s)
Humans , Male , Anal Canal/abnormalities , Rectum/abnormalities , Syndrome , Rectal Diseases/congenital , Anus Diseases/congenital , Infant, Newborn, Diseases
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