Show simple item record

dc.contributor.authorGoksel, S
dc.contributor.authorIlvan, S
dc.contributor.authorDervisoglu, S
dc.contributor.authorRamazanoglu, R
dc.contributor.authorAksoy, F
dc.date.accessioned2021-03-05T16:35:34Z
dc.date.available2021-03-05T16:35:34Z
dc.date.issued2000
dc.identifier.citationAksoy F., Goksel S., Ilvan S., Dervisoglu S., Ramazanoglu R., "Congenital generalized infantile myofibromatosis and neonatal hemochromatosis - An autopsy case report", TURKISH JOURNAL OF PEDIATRICS, cilt.42, ss.334-337, 2000
dc.identifier.issn0041-4301
dc.identifier.othervv_1032021
dc.identifier.otherav_c161e521-1130-409c-a5c3-2a7bfe14c9d1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/128344
dc.description.abstractAn autopsy case of congenital infantile myofibromatosis and neonatal hemochromatosis is reported. A thirty-six-hour-old baby girl had multiple subcutaneous nodules in addition to multiple visceral involvement of heart, lungs, pharynx, larynx, stomach, small bowel, large bowel, pancreas, kidneys, spleen, thyroid, adrenal glands, lymph nodes, peripheral nerves, meninges and soft tissues. In these tumoral nodules, three types of histological patterns were observed: 1-hemangiopericytoma-like, 2-mixed, and 3-pure spindle cell. Tumor cells were immunohistochemically positive for actin, and negative for desmin, muscle-specific antigen, and estrogen, related protein. The histological and immunohistochemical findings of the case suggested that a close relationship may exist between infantile myofibromatosis and infantile hemangiopericytoma. In addition to infantile myofibromatosis, neonatal hemochromatosis characterized by iron deposition in parenchymatous organs such as liver, pancreas, lungs, thyroid, and adrenal glands was another important characteristic of the case.
dc.language.isoeng
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleCongenital generalized infantile myofibromatosis and neonatal hemochromatosis - An autopsy case report
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF PEDIATRICS
dc.contributor.department, ,
dc.identifier.volume42
dc.identifier.issue4
dc.identifier.startpage334
dc.identifier.endpage337
dc.contributor.firstauthorID126575


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record