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Biomedical subjects

D Träger

Publications and source records attributed to D Träger.

26 records · Page 2Linked to original sources

[Caudal regression syndrome].

It is reported about a young girl with congenital agenesis of the os sacrum, a congenital platfoot and a luxation of the left hip. These congenital malformations can be found in children born to diabetic mothers.

Abnormalities, Multiple↗

[Malignant hemangiopericytoma--a soft tissue and bone tumor].

Hemangiopericytomas are very rare tumors that mostly develop in the soft tissues. In rare cases, however, they may occur as primary bone tumors which are extremely rare. In case of such an intraosseous tumor, a bone metastasis of such a soft tissue sarcoma must be considered first and has to be excluded. In a 62 year old female, a hemangiopericytoma of the left femoral neck was diagnosed that had induced a pathological bone fracture. A resection of the femoral head and neck was performed. Anamnestical investigations, however, have shown that 4 years before, such a tumor of the pelvic soft tissues was removed. Thus, the lesion of the femoral neck had to be classified as bone metastasis of a malignant hemangiopericytoma. It has to be emphasized that this special tumor always shows a questionable prognosis and, by histological investigations, it cannot be decided if we are dealing with a benign or malignant tumor growth. Diagnostic managements and clinical problems with hemangiopericytomas are discussed in detail.

Female↗

[Dysontogenetic blockbuilding of the vertebrae at the lumbo dorsal junction].

It is reported in two cases of synostosis of the vertebral which is related in the Medical literature as "Dysontogenetic blockbuilding of the Corpus Vertebrae". This condition could be seen in a 13 year old boy in the area of Th 9 to Th 12 and in a 13 year old girl from Th 11 to L1. The clinical and radiological findings of these two cases will be described and discussed. An attribution of these cases to the "Dysontogenetic blockbuilding" groups was based on a disturbance of the vertebral forming. A causal therapy is not possible.

Adolescent↗

[Spontaneous idiopathic osteolysis (Gorham syndrome). A case report].

The spontaneous idiopathic osteolysis is know as a slow progressive absorbtion process of the bone with unknown causes. It is supposed that in the "Gorham-Syndrom" a hämangiomatosis of the bone exists. In some cases of spontaneous osteolysis there wasn't any vascular proliferation noted. One case with spontaneous osteolysis will be discussed. The histological picture of this patient is described as a chronic uspecific osteoarthritis. Another case could be documented radiologically at the left distal ulna. The attribution of these cases to the "Gorham-Syndrom" is discussed.

Biopsy↗