Presacral Cystic Neuroblastoma: Case Report and Review of the Literature
Пресакральная кистозная нейробластома: описание клинического случая и обзор литературы
2006-08-01
SCID: 54.1/zm8d8vv9
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N-myc amplificationcystic neuroblastomainfant neuroblastomapelvic neuroblastomapresacral tumor
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Abstract (AI)
Cystic neuroblastoma (CN) is highly unusual; since 2005 only 55 cases have been reported in the medical literature. The authors report a case of pelvic (presacral) CN in a 2-month-old boy. Computed tomography scan confirmed a cystic, septated, and encapsulated mass. Complete tumor excision was achieved. Histopathology diagnosed a stroma-poor and undifferentiated neuroblastoma with multiple calcifications. meta-iodobenzylguanidine scan, radionuclide bone, and a bone marrow aspiration were normal. N-myc amplification was absent. The infant was classified stage I neuroblastoma and received no further therapy (4 y of follow-up). To the authors' knowledge, this is the first report of a CN in a pelvic-presacral location.
Key Findings
1
Computed tomography revealed a cystic, septated, encapsulated pelvic mass, which was completely excised.
2
Histopathology showed a stroma-poor, undifferentiated neuroblastoma with multiple calcifications.
3
Staging investigations were negative, including meta-iodobenzylguanidine imaging, radionuclide bone scanning, and bone marrow aspiration; N-myc amplification was absent.
4
The infant was classified as stage I neuroblastoma, received no additional therapy, and remained under follow-up for four years.
5
The report describes a rare presacral cystic neuroblastoma in a 2-month-old boy, representing the first reported pelvic-presacral case.
Research Object
Pelvic (presacral) cystic neuroblastoma in a 2-month-old boy
Research Subject
Clinical, pathological, molecular, and follow-up characteristics and treatment outcome of the cystic neuroblastoma
Publication Details
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2006-08-01
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