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Yenidoğan Döneminde Nöron Spesifik Enolaz Yüksekliği ile Seyreden Atipik (Selüler) Konjenital Mezoblastik Nefroma Olgusu
Author(s) -
Nihan Hilal Hoşağası,
Dílek Díllí,
İsmet Faruk Özgüner,
Gürses Şahin,
Esin Cengiz Boduroğlu,
Banu Aydın,
Nuran Üstün,
Ayşegül Zencıroğlu,
Nurullah Okumuş,
Burak Özkan
Publication year - 2014
Publication title -
haseki tıp bülteni
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.113
H-Index - 4
eISSN - 2147-2688
pISSN - 1302-0072
DOI - 10.4274/haseki.1577
Subject(s) - medicine
The most common causes of abdominal mass are neuroblastoma, germ cell tumors, hepatoblastoma and congenital mesoblastic nephroma. Congenital mesoblastic nephroma (CMN) accounts for more than 90% of all renal tumors seen in the first three months of life. Total nephrectomy is curative. Neuron-specific enolase is a glycolytic enzyme that is localized primarily to the neuronal cytoplasm. Its sensitivity is especially high for neuroblastoma and small cell lung cancer. In this paper, we report a newborn with abdominal mass that was firstly considered as neuroblastoma due to calcifications observed on ultrasonography and high levels of serum neuron-specific enolase. After histopathological evaluation of the lesion, the patient was diagnosed as having atypical (cellular) congenital mesoblastic nephroma. (The Me­di­cal Bul­le­tin of Ha­se­ki 2014; 52: 223-6

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