The most common location for neuroblastoma

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The maximum not unusual location for neuroblastoma to originate (i.E., the number one tumor) is inside the adrenal glands. This takes place in 40% of localized tumors and in 60% of cases of massive disease. Neuroblastoma can also broaden anywhere alongside the sympathetic frightened machine chain from the neck to the pelvis. Frequencies in one-of-a-kind locations encompass: neck (1%), chest (19%), stomach (30% nonadrenal), or pelvis (1%). In rare instances, no number one tumor may be discerned.

Rare however feature displays include transverse myelopathy (tumor spinal cord compression, 5% of cases), treatment-resistant diarrhea (tumor vasoactive intestinal peptide secretion, 4% of instances), Horner's syndrome (cervical tumor, 2.4% of cases), opsoclonus myoclonus syndrome and ataxia (suspected paraneoplastic purpose, 1.3% of cases), and hypertension (catecholamine secretion or kidney artery compression, 1.3% of cases).