Accepted at 5:55 p.m. Oct, 31, 2023 by Alex
Author: Kaedon
Related Note: 1482886913645
Rationale for change

AMBOSS details more specifics for classifying types of CNS tumors Turcot syndrome presents with

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Pathoma
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Pixorize

Review Familial Adenomatous Polyposis (FAP)
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OME

Additional Resources

Medulloblastoma
T2-weighted cranial MRI (axial view) of a 7-year-old boy: isodense round lesion with hyperintense sections in the fourth ventricle (green overlay); grossly diminished gyration of the cerebellum (C). (P = poorly demarcated pons region; B = basilar artery, CS = external CSF space)



Medulloblastoma
T1-weighted cranial MRI of a 6-year-old child presenting with features of increased intracranial pressure (midsagittal section with contrast)
There is a large hypointense mass occupying the third (upper yellow overlay) and fourth (lower yellow overlay) ventricles that is causing obstructive hydrocephalus (pink overlay).
The pink overlay also highlights the leakage of CSF into the periventricular space (transependymal edema) and into the occipital lobe due to the increased intraventricular pressure.
This appearance of a fourth ventricular mass in a child is characteristic of medulloblastoma.



Medulloblastoma
Cranial MRI (T1-weighted, with contrast)
There is a mass in the posterior cranial fossa. It features solid parts (green overlay) and cystic parts (red overlay).
Location and appearance are typical of a medulloblastoma.

(D: diencephalon; P: pons; C: cerebellum; yellow outline: cerebellar tentorium)



Medulloblastoma
Photomicrograph of cerebellar vermis tissue (H&E stain)
Densely packed, small, blue anaplastic cells are present throughout the specimen. The cells have pleomorphic and hyperchromatic nuclei.
On the right, a vessel (its lumen mostly obstructed by eosinophilic material) can be seen.
These are typical histopathological findings of medulloblastoma.



Medulloblastoma
Photomicrograph of cerebellar vermis tissue (H&E stain)
Numerous small, blue, round cells with scant cytoplasm can be seen throughout the specimen (classic examples: arrows, green overlay). Their nuclei vary in size and structure (nuclear pleomorphism) and many cells feature distinctly hyperchromatic nuclei.
The majority of the cells are arranged in concentric clusters around lighter central areas consisting of neuropil (examples: dashed outlines and yellow overlay, magnified area). These clusters are referred to as Homer Wright rosettes.
These histopathological features, particularly the Homer Wright rosettes, are characteristic of a medulloblastoma.

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#AK_Step1_v12::#OME::04_Organ_Systems::03_Gastrointestinal::01_Digestion_&_Absorption::12_Neoplasia_of_Large_Intestine #AK_Step1_v12::#B&B::09_GI::03_Clinical::14_Colon_Cancer #AK_Step1_v12::#OME::Clinical::04_Organ_Systems::03_Gastrointestinal::01_Digestion_&_Absorption::12_Neoplasia_of_Large_Intestine #AK_Step1_v12::#FirstAid::09_Gastrointestinal::04_Pathology::25_Polyposis_Syndromes::Turcot_Syndrome #AK_Step1_v12::#SketchyPath::05_GI::03_Colorectal_&_Anal_Disorders::03_Colorectal_Polyps_&_Cancer !AK_UpdateTags::Step1decks::Zanki-Step-Decks::Zanki-GI::GI-Pathology #PANCE::EOR::Family_med #AK_Step2_v12::#B&B::06_Gastroenterology::04_Intestines::01_Colon_Cancer #AK_Step1_v12::#Pixorize::01_Biochemistry::22_Misc::06_Familial_Adenomatous_Polyposis_(FAP) #AK_Step1_v12::^Other::^HighYield::2-RelativelyHighYield #AK_Step1_v12::^Systems::GI::pathology #AK_Step2_v12::#OME::01_Medicine::03_Gastroenterology::11_Colon_Cancer #AK_Step1_v12::#Pathoma::10_GI::08_Colon #AK_Step2_v12::#Resources_by_rotation::IM::ome::gi::colon_cancer #AK_Step2_v12::#SketchyIM::10_Gastroenterology::03_Colorectal_Cancer::01_Colon_Cancer_Carcinogenesis #AK_Step2_v12::#B&B::16_Surgery_&_Anesthesia::03_Related_Videos::05_Colon_Cancer #AK_Original_Decks::Step_1::Zanki_Step_Decks::Zanki_GI::GI_Pathology #AK_Step1_v12::#Bootcamp::Gastroenterology::09_Colorectal_Pathology::09_Hereditary_Polyposis #PANCE::GI::colorectal_disorders