Interactive Transcript
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Dr. P here.
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3 00:00:01,750 --> 00:00:02,500 Yeah, you're right.
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This is not an MRI.
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It's an axial CT of a three-year-old.
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And I've included it in the renal section
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because it's right in the neighborhood and
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often comes into the stream of consciousness
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for medical students, residents, fellows,
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and board takers, people taking an exam.
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So I'll just spend three minutes or less
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talking about this calcified lesion, which
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calcifies 85% of the time, neuroblastoma.
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It's a complex, heterogeneous disease
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that we'll cover in the adrenal section.
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It arises from the embryonic cells that form the
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primitive neural crest, with a natural history ranging
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from a benign course to a terminal illness.
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In recent years, there are a number of genetic
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techniques that have been used to stratify
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patients according to risk of metastasis, and/or death.
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23 00:00:50,470 --> 00:00:54,571 Neuroblastoma, ganglioneuroblastoma, and ganglioneuroma
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comprise a spectrum of disorders
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that arise from primitive sympathetic
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ganglion cells called neural crest cells.
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Overall, approximately 46% of neuroblastomas,
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almost half, arise from the adrenal gland,
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and that's a potential board question.
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18% arise from extra-adrenal abdominal
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locations, and 14% arise from the posterior mediastinum,
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or the thorax, and the remainder
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from the head, neck, pelvis, and other locations.
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But probably another very important
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board issue is neuroblastoma represents
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97% of all neuroblastic tumors,
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and it's the third most common childhood cancer.
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It is the most common extracranial
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solid tumor of childhood.
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Calcified adrenal mass on the right side, seen on CT.
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It doesn't come from the kidney;
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it comes from the adrenal neuroblastoma.
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Dr. P out.
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