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Biomedical subjects

D Hörmann

Publications and source records attributed to D Hörmann.

At least 19 recordsLinked to original sources

[Bacterial bone and joint infections in childhood--a review. 4. Subacute and primary-chronic osteomyelitis, rare forms of osteomyelitis].

This is an overview of the most important aspects of pathogenesis, etiology, diagnostics, therapy and differential diagnostics of the subacute and primary chronic osteomyelitis in children. This group of disease includes Brodie's abscess, plasma cellular osteomyelitis, sclerosing osteomyelitis (Garré) and the chronic recurrent multifocal osteomyelitis. The treatment of children with these not completely understood diseases requires a close cooperation between pediatricians, pediatric surgeons and radiologists.

Adolescent

[The clinical relevance of the dynamics of ventricular changes in surgically treated hydrocephalus of children with myelomeningocele].

The normalisation of head circumference and ventricular dilatation are aims of the therapy of hydrocephalus. Sonographic follow-up after ventriculo-peritoneal shunt demonstrates a changed ventricular morphology and inform about clinical relevant questions in regard of effectivity and complications of the shunt. The different morphological development of liquor systems in spite of comparable premises is discussed on the base of 47 children with myelomeningoceles.

Cephalometry

[Bronchopulmonary foregut malformations with communication to the esophagus].

Congenital abnormal communications between separated pulmonary tissue and the oesophagus are rarities. Only about 50 cases have been reported in the literature. For all different forms the term of bronchopulmonary foregut malformation (BPFM) was first applied by Gerle and his coworkers in 1968. Major symptoms of this condition involved respiratory distress, cough, dyspnea, vomiting and repeated pneumonia. This paper presents reports of two own patients. In both cases was confirmed a bronchopulmonary foregut malformation in the lower right thorax with ectopic main bronchus communicating into the distal oesophagus. According to the literature we describe our own experience and discuss embryologic pathogenesis and surgical consequences for children.

Bronchial Fistula

[Results of cerebral sonography in children with myelomeningoceles].

47 infants with myelomeningocele were investigated by ultrasound after the surgical closure of the cele and followed up to 12 months. The aim was the early diagnosis of hydrocephalus and the recording of morphological features of the ventricular system in comparison with hydrocephali of other origins, especially of Chiari-Syndrome. 31 infants needed a shunt due to rapid progress of the ventricular dilatation and clinical signs of a raised intracranial pressure: in 25 of this group (81%) the ultrasound investigation demonstrated a Chiari-Syndrome. Of 16 further infants who definitely did not need a shunt, only 5 (31%) had a Chiari-Syndrome. Therefore, the first sonographic examination seems to provide a certain prognostic evidence for the development of a hydrocephalus.

Arnold-Chiari Malformation