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Titlebook: Neuroradiology - Images vs Symptoms; Martina ?pero,Hrvoje Vavro Book 2021 The Editor(s) (if applicable) and The Author(s), under exclusive

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樓主: Novice
31#
發(fā)表于 2025-3-27 00:41:25 | 只看該作者
32#
發(fā)表于 2025-3-27 05:09:31 | 只看該作者
CAPNON: Calcifying Pseudoneoplasm of the Neuraxistors such as trauma, infection, inflammation or degeneration. Classic imaging features include a well-defined calcified mass lesion on CT, hypointense in MRI images, with minimal or completely without perifocal oedema, possibly with a rim of gliosis and/or mild peripheral enhancement.
33#
發(fā)表于 2025-3-27 08:05:28 | 只看該作者
Thrombotic Thrombocytopenic Purpura (TTP) and Haemolytic-Uremic Syndrome (HUS)c haemolytic anaemia, thrombocytopenia and microthrombi leading to ischaemic tissue injury. In TTP, CNS is the most affected organ, whereas in HUS it is kidneys. CNS imaging findings in TTP range from normal to PRES, ischaemia and haemorrhage. Therapeutic plasma exchange (TPE) is the mainstay of TTP treatment.
34#
發(fā)表于 2025-3-27 11:03:21 | 只看該作者
Intraventricular Meningiomaes. Trigonal meningiomas grow silently for a long period of time due to the relatively ample ventricular space available. GTR is the treatment of choice; recurrences are possible in WHO grade II tumours, therefore requiring more frequent MRI follow-ups in the first 2?years.
35#
發(fā)表于 2025-3-27 17:13:49 | 只看該作者
36#
發(fā)表于 2025-3-27 20:32:24 | 只看該作者
37#
發(fā)表于 2025-3-27 22:47:02 | 只看該作者
38#
發(fā)表于 2025-3-28 04:08:51 | 只看該作者
39#
發(fā)表于 2025-3-28 10:03:40 | 只看該作者
Pilocytic Astrocytoma at the L1–L2 LevelIn 2018, a 50-year-old male patient came for MRI of the lumbar spine as an outpatient. MRI was recommended by neurologist due to bilateral, mainly left-sided radiculopathy with radicular pain and weakness in the left leg lasting for several months (Fig. 10.1).
40#
發(fā)表于 2025-3-28 13:14:49 | 只看該作者
Antiphospholipid Syndrome in a Patient with Systemic Lupus Erythematosus ElementsIn 2019, a 52-year-old female patient was hospitalized due to diagnostic work-up of suspected antiphospholipid syndrome and suspected lupus nephritis.
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