Giant Intracranial Xanthoma with Cloudy Vision as the First Symptom: A Case Report and Literature Review.

A 31-year-old male with mild dizziness complained of cloudy vision in his right eye for 5 days. The visual acuity of both eyes was normal, while the visual contrast sensitivity of both eyes slightly reduced. Fundus examination showed the swollen and radial superficial hemorrhage of his both optic nerves. Brain MRI scan indicated a huge tumor in the right temporal lobe with clear boundary, close to the skull. The midline structure shifted to the left. Blood tests indicated no hyperlipidemia or lipid disorders. The patient then received tumor resection. The size of the tumor was 5.6 cm × 7.5 cm × 10.1 cm. Histology suggested many foam cell accumulations and the tumor was positive for CD34, CD99, Vimentin, β-Catenin and CD68, but negative for EMA, GFAP, IDH-1, Oliga-2, PR, S-100, and CD1a. Three months after surgery, MRI showed the midline structure was back to normal. The swollen and radial superficial hemorrhage of optic nerves had disappeared. The visual acuity and visual field remained normal.

A 31-year-old male complained of blurred vision in his right eye for five days, accompanied by mild dizziness. The visual acuity of both eyes was 20/20. The visual contrast sensitivity of both eyes reduced slightly. No yellowish nude in the eyelid and elsewhere. No obvious abnormalities in the conjunctiva, cornea, anterior chamber, iris, or lens of either eye. The pupil size of both eyes was 2.5 mm, RAPD (-). Fundus examination showed the swollen and radial superficial hemorrhage of his both optic nerves. (Figure 1A and B). Blood examination showed the total cholesterol, triglycerides, high density lipoprotein and low-density lipoprotein were within the normal limits. Brain MRI showed a huge mass in the right temporal lobe, clear boundary, and multiple separations. The right temporal lobe and lateral ventricle were compressed, the midline structure shifted to the left. The lesion site showed low signal intensity on T1-weighted images (Figure 2A) and high signal intensity on T2-weighted images (Figure 2B). Contrast-enhanced T1-weighted images showed strong enhancement at the boundary (Figure 2C and D). The patient then received tumor resection. During the operation, we found the skull around the tumor area was partially protruding; the tumor had invaded the skull; the adhesion of tumor and skull was tight. The size of the tumor was about 5.6 cm × 7.5 cm × 10.1 cm, and the texture was soft and gelatinous (Figure 3). Histology showed a large number of foam cell accumulation (Figure 4). The immunohistochemistry was as follows: CD34 (+), CD99 (+), Vim (+), CD68 (+), β-Catenin (+), EMA (−), GFAP (−), IDH-1 (−), Oliga-2 (−), PR (−), S-100 (−), CD1a (−), Ki-67 index was about 10%. Three months follow up showed the visual acuity and visual fields remained normal. The optic disc edema and hemorrhages had disappeared (Figure 1C and D). T1-weighted (Figure 5A) and T2-weighted (Figure 5B) images show the midline structure returned to normal. A mild edema of temporoparietal was observed (Figure 5A and B). Contrast-enhanced T1-weighted images (Figure 5C and D) show no sign of recurrence.

Figure 1

Fundus photography. The swelling and blurry boundaries of both optic nerves were present (A and B). There was a splinter radial superficial retinal hemorrhage above the optic disc; no other obvious abnormality was observed (A and B). Three months after surgery, all these symptoms, including optic nerve swelling and retinal hemorrhage disappeared (C and D).

Figure 2

Brain MRI before surgery. Brain MRI showed a huge mass in the right temporal lobe, clear boundary, and multiple separations. The right temporal lobe and lateral ventricle were compressed, the midline structure shifted to the left (A and B). The lesion site showed low signal intensity on T1-weighted images (A) and high signal intensity on T2-weighted images (B). Contrast-enhanced T1-weighted images showed strong enhancement at the boundary (C and D).

Figure 3

Surgical observations. The skull in the tumor area was partially protruding, the tumor invaded the skull, the adhesion of tumor tissue and skull was tight and the brain tissue of the right temporal lobe was compressed (A). The actual size of the tumor was 5.6 × 7.5 × 10.1 cm, and the texture was soft and gelatinous (B and C).

Figure 4

Hematoxylin and eosin staining. Foam cell accumulation in the mucous connective tissue of the right temporal lobe.

Figure 5

Three-month follow-up (MRI). T1-weighted and T2-weighted images show the midline structure returned to normal. A mild edema of temporoparietal was observed (A and B). Contrast-enhanced T1-weighted images (C and D) show no sign of recurrence.

Written informed consent was obtained from the patient for the publication of the case details and images. No institutional review board approval was required for the publication of the case report.

Discussion

Xanthomas are produced by the accumulation of foam cells which originate from the oxidation of macrophages overloaded with low-density lipoprotein particles. Generally, Xanthomas can be divided into three types: both hyperlipidemia xanthoma1 and non-hyperlipidemia xanthomas2 contain lipids and collagen, whereas progressive collagen necrosis, cholesterol crystal fissures and lipid vacuoles can be seen in the tissue examination of necrobiotic xanthogranuloma.3,4 Xanthomas have a variety of clinical manifestations, depending on the location of lesions. The most common cases show yellowish collection of cholesterol underneath the skin, usually on or around the eyelids.5 Although intracranial xanthoma is not a rare condition,6–9 the huge size of tumor without hyperlipidemia or lipid disorders has never been reported.

Xanthomas are associated with a variety of diseases, especially lipid-storage and metabolism disorders, which often occur in patients with type II hyperlipidemia. Since its mechanism is similar to that of early atherosclerosis, xanthoma has received more attention in recent years. A prospective study, which followed nearly 13,000 subjects for more than 20 years, found that, even after adjusting for covariables such as age, gender, diabetes, smoking, hypolipidemic therapy and postmenopausal status, the occurrence of xanthoma was associated with: a significant increase in the risk of myocardial infarction (48% increase); ischemic heart disease (38% increase); and lower-extremity ischemic disease (70% increase).10 To-date, most of the reported intracranial xanthomas have been characterized by hyperlipidemia, especially type II hyperlipidemia. There was also a report of a young patient with bilateral disc swelling caused by intracranial xanthoma. But, the patient had severe hyperlipidemia, and the patient’s mother and two sons had elevated blood lipids.11 However, hyperlipidemia or lipid disorder was not found in this case.

The diagnosis and differential diagnosis of intracranial xanthoma majorly rely on histology and immunohistochemistry findings. No accurate diagnosis can be determined until operation. The giant foam cells drive from macrophages but not from smooth muscle cells, neural cells or the transformation of epithelial cells.12 Thus, in this case, the tumor was positive for CD68 and Vimentin, commonly used macrophage markers13,14 and CD99 which plays a key role in the migration of macrophages through endothelial junctions15 and β-Catenin which regulates macrophage activation.16 In contrast, this tumor was negative for makers of neural origin: S-100,17 GFAP,18 Oliga-219 and IDH-1.20 Also, since xanthomas are apparently not true neoplasms,21 it is negative for PR22 and CD1a.23

Because the incidence of intracranial xanthoma is low, no systematic study shows the recurrence rate and prevention for this disease. Theoretically, reducing blood triglyceride and cholesterol levels might be beneficial for this tumor.24 Long term, large number observation study might be needed.