June 1986, Volume 36, Issue 6

Case Reports

LIPOMA OF CORPUS CALLOSUM DIAGNOSED BY CT SCANNING - A CASE REPORT

Ali Jumshyd  ( National X-Ray and Ultrasound Centre, Karachi. )
S. Tariq Sohail  ( Medicare Hospital, Karachi. )

Abstract

Lipoma of corpus callosum is a rare intracranial tumour or malformation. The appea­rances of this tumour in computerised tomo­graphy (CT) brain scans are fairly specific. A case report is presented with a short discussion of reported cases and review of literature and CT features of the tumour (JPMA 36: 149, 1988).

CASE REPORT

A 25 years old male was admitted under the care of psychiatrist in a private hospital in Karachi with complaints of headache off and on for 10 years; sleep disturbances and night terrors, abnormal body posture and social phobias for the last 1½ years. Past history was non-contributory. He was an occasional smoker and had studied uptill Intermediate College level. General and system examination was unremarkable. Laboratory investigations showed Haemoglobin 11.8 Gms, ESR 23mm, normal leucocyte count and negative urine examination. Skull X-Rays did not show pathological calcification or any other abnormality.
CT FINDINGS
CT scanning of the brain done four days after admission at the same Hospital on a Head and Body scanner showed a large area of decreased attenuation situated in the midline in the region of the corpus callosum. The lateral ventricles were parallel in position and were not dilated as shown in the figure.


The low density area showed fatty density with small flecks of calcification at the peri­phery of the lesion.
Diagnosis of lipoma of corpus callosum was made and the patient was referred to the Neuro­surgeon who thought it inadvisable to remove the whole tumour. Biopsy was taken and histopatho­logical findings confirmed the lesion as lipoma of corpus callosum.

DISCUSSION

Intracranial lipomas are rare tumours. The most frequent site is corpus callosum, but they also occur in the cerebellopontine angle and quadrigeminal plate cisterns1. They are frequently associated with absence of septum pellucidum and corpus callosum, cervical spine anomalies, myelomeningocoele, spina bifida and agenesis of cerebellar vermis.
According to Gastaut, Regis et a12 only 100 cases have been published since the original observation of Rokitansky in. 1856. These authors have reported four cases of Lipoma of corpus callosum with epilepsy detected by CT from amongst 13,000 patients (0.03%).
Kazner and Stochdorph’1 have reported 11 cases found within four years among 17,500 patients who were studied by CT scanning. Iñtra­cranial lipomas can produce symptoms. In the series published by Kazner and Stockdorph3 eight of 11 patients, presented with symptoms that may be directly or indirectly related to intra­cranial lipoma. They can produce hydrocephalus with signs of raised intracranial pressure. Gastaut2 reported cases associated with epilepsy. Our case also showed some non specific symptoms mainly behavioural anomaly.
CT findings4 are an area of low attenuation situated in the midline with irregular margins and with tharp demarcation. The density of these lesions is between -50 to 150 Houns­field units. Linear calcification are frequently identified at the margins of these tumours. Con­trast enhancement occurs only within the dilated and tortuous anterior cerebral artery which penetrates these corpus callosal tumours but does not extend within substance of the tumour. Over haif of these tumours are associated with partial or complete agenesis of corpus callosum 4. Differential diagnosis is mainly with dermoid tumours but these are cystic lesion in the midline and in a particular situation. The cysts are thick walled with calcification and teeth or dense calci­fication inside the cyst. CT demonstrates the cyst wall as isodense with adjacent brain except where it is calcified. If these rupture, fat fluid levels may occur and CT features of dermoid cysts are also fairly specific.
The case presented illustrates the fairly specific features of lipoma of corpus callosum and almost definitive diagnosis can be made on CT scanning. With increasing use of CT scanners, it is hoped that more cases of this rare condition will be reported.

REFERENCES

1. Faerber, E.N. and Wolpert, S.M. The value of computed tomography in the diagnosis of intra­cranial ipomata. J. Comput. Assist. Tomogr., 1978; 2: 297.
2. Gastaut, H., Regis, H., Gastaut, J.L. , Yermenos, E. and Law , M.D. Lipomas of the corpus callosum and epilepsy. Neurology, 1980; 30: 132.
3. Kazner, E., Stochdorph, 0., Wende, S. and Grumme, T. Intracranial lipoma; diagnostic and therapeutic considerations. J. Neurosurg., 1980; 52: 234.
4. Haaga, J.R. and Alfidi, R.J. Computed tomography of the whole body. St. Louis, Mosby, 1983; p.90.

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