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1 All authors: Department of Radiology, Emory University School of Medicine, B-115, 1364 Clifton Rd. NE, Atlanta, GA 30322.
Received September 11, 2007;
accepted after revision April 25, 2008.
Address correspondence to A. Jayashankar
(ajayash{at}emory.edu).
Abstract
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Keywords: hemorrhagic neoplasms intracranial hemorrhage intracranial metastases metastatic melanoma MRI
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| QUESTION 1 Which of the following primary neoplasms is NOT typically
associated with hemorrhagic brain metastases?
QUESTION 2 Hemorrhagic neoplasms constitute approximately what percentage of intraparenchymal hematomas?
QUESTION 3 Which of the following statements regarding the MRI features of hemorrhagic neoplasms as compared with nonneoplastic intraparenchymal hematomas is FALSE?
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Solution to Question 1
Hemorrhagic brain neoplasms include both primary brain tumors and
metastases. A hemorrhagic neoplasm is far more likely to be metastatic than
primary [1]. Metastases that
are most likely to hemorrhage include lung, breast, thyroid, renal cell,
choriocarcinoma, and malignant melanoma
[1]. Options A, C, D, and E are
not the best responses. Metastases to the brain from prostate cancer are rare
and are not typically associated with hemorrhage. Option B is the best
response.
| QUESTION 4 Which structure is most commonly involved by melanoma that
metastasizes to the head?
QUESTION 5 The melanotic imaging pattern of metastatic melanoma is most typically associated with which of the following signal characteristics?
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Solution to Question 2
Hemorrhagic neoplasms constitute approximately 1–14% of all
intraparenchymal hematomas [2].
Option A is the best response.The differential diagnosis for the
remainder of intraparenchymal hematomas includes primarily hypertensive
hemorrhage, vascular anomalies (including arteriovenous malformation and
cavernous malformation), hemorrhagic infarction, amyloid angiopathy, and
trauma.
Solution to Question 3
Imaging features on MRI that suggest hemorrhagic neoplasm rather than
benign intraparenchymal hematoma includes a heterogeneous or mixed intensity
pattern (Option D); an incomplete hemosiderin rim (Option A);
disproportionately large amount of edema compared with hematoma size,
persistence of or increase in the edema over several days or weeks (Option C);
persistence of T2 hypointensity beyond the expected time for a nonneoplastic
hematoma (Option B); and initial appearance of T1 hyperintensity (subacute
methemoglobin) centrally or eccentrically in the hematoma. Options A, B, C,
and D, are not the best responses since they are true statements. In contrast,
nonneoplastic hematomas usually show initial methemoglobin formation at the
periphery of the hematoma [2,
3]. Although the precise
mechanisms for the formation of methemoglobin have not been elucidated, it has
been hypothesized that low oxygen tension levels favor the formation of
methemoglobin. In a hemorrhagic neoplasm, low oxygen tension levels are found
centrally, presumably in the necrotic portions of the tumor. For this reason,
it is thought that methemoglobin formation initially occurs centrally (or
eccentrically) in a hemorrhagic neoplasm rather than at the periphery
[2]. Therefore, Option E,
which is not true, is the best response.
Solution to Question 4
Melanoma metastatic to the head can involve virtually any intracranial or
extracranial structure, including the meninges, orbit, nasopharynx, internal
auditory canal, choroid plexus, bone, muscle, and meninges. However, the brain
is the most common site of metastases to the head from melanoma
[4]. Option A is the best
response.Options B, C, D, and E are not the best responses.
Solution to Question 5
Two classic imaging patterns have been described for melanoma metastatic to
the brain based on signal intensity characteristics. The melanotic form is
characterized by T1 hyperintensity and T2 hypointensity. Option B is the
best response. The amelanotic form is characterized by T1 hypointensity
and T2 hyperintensity. Although some studies have shown high specificity of
the melanotic imaging pattern for melanin-containing metastases
[5], the association
nevertheless remains controversial. The amelanotic imaging pattern is
nonspecific. Gaviani et al. [6]
studied the use of T2* images (susceptibility sequences) in the imaging of
metastatic melanoma to the brain and reported a high specificity of combined
T1 hyperintensity and T2* hypointensity for melanoma metastases. The
classically described melanotic pattern, however, is based on the T1 and T2
signal characteristics only. Options A, C, D, and E are not the best
responses.
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