Primary Intrarenal Neuroblastoma with Hypertension and Disseminated Intravascular Coagulation
| Autor: | Mohammad Taghi Arzanian, Nima Rezaei, Bibi Shahin Shamsian, Roxana Azma, Nozar Ghojehvand, Farid Ghazizadeh, Mohsen Rouzrokh, Seyed Malek Mesbah, Maryam Kazemi Aghdam, Mohammad Kajizadi |
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| Rok vydání: | 2013 |
| Předmět: |
Disseminated intravascular coagulation
Fetus Pathology medicine.medical_specialty business.industry Case Report Mediastinal mass Adrenal neuroblastoma lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens medicine.disease lcsh:RC254-282 Rare tumor Oncology Neuroblastoma medicine business Pathological correlation |
| Zdroj: | Case Reports in Oncological Medicine Case Reports in Oncological Medicine, Vol 2013 (2013) |
| ISSN: | 2090-6714 2090-6706 |
| DOI: | 10.1155/2013/684939 |
| Popis: | The primary intrarenal neuroblastoma (IRNB) is a rare condition. Intrarenal neuroblastoma typically results from direct renal invasion from an adrenal neuroblastoma, but true intrarenal neuroblastoma originates either sequestered adrenal rests during the fetal life or intrarenal sympathetic ganglia. Clinical, radiological, and pathological correlation is very essential for diagnosis and appropriate management of this type of unusual cases. The distinction of this rare tumor from Wilms’ tumor is an important challenge since both tumors have major differences in prognostic and therapeutic response. We present a 3-year-old boy of primary intrarenal neuroblastoma with extensive abdominal and mediastinal mass, persistent hypertension, and disseminated intravascular coagulation (DIC). |
| Databáze: | OpenAIRE |
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