Fahr's Disease With Intracerebral Hemorrhage at the Uncommon Location: A Case Report
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Updated: Aug 16, 2026

Minimally Invasive Endoscopic Intracerebral Hemorrhage Evacuation
Published on: October 15, 2021
Baek Hee Jang1, Seong Wook Son1, Chung Reen Kim1
1Department of Physical Medicine and Rehabilitation, Ulsan University Hospital, Ulsan, Korea.
Insights
Fahr's disease, a rare neurologic condition, involves brain calcification. This case highlights an unusual hypertensive hemorrhage location, potentially due to calcification in common hemorrhage sites.
Area of Science:
- Neurology
- Radiology
- Genetics
Background:
- Fahr's disease (FD) is a rare neurologic disorder characterized by symmetric, bilateral intracerebral calcification.
- It often presents with diverse neurological symptoms, making diagnosis challenging.
Observation:
- A 65-year-old woman presented with gait disturbance, altered mentality, and visual field defects.
- Brain CT revealed spontaneous intracranial hemorrhage and bilateral intracerebral calcification.
- Laboratory tests indicated hypoparathyroidism, and her son also had similar calcifications, confirming FD.
Findings:
- The patient had hypertension, a potential cause of hemorrhage.
- However, the hemorrhage occurred in an uncommon parieto-occipital location, away from heavily calcified areas.
- Massive calcification in the basal ganglia may have prevented hemorrhage in typical locations, redirecting it elsewhere.
Implications:
- This case expands the understanding of Fahr's disease presentation and potential hemorrhage patterns.
- It suggests that extensive intracranial calcification might influence the location of hypertensive hemorrhages.
- Further research is needed to elucidate the relationship between calcification burden and hemorrhage site in FD.
Abstract:
Fahr's disease (FD) is a rare neurologic disorder characterized by the symmetric and bilateral intracerebral calcification in a patient. We describe the case of a 65-year-old woman who presented with gait disturbance, abnormal mentality, and visual field defect. The result of a brain computerized tomography showed spontaneous intracranial hemorrhage in the right parieto-occipital area, and also showed the incidence of symmetric and bilateral intracerebral calcification. Moreover, laboratory studies indicated characteristic hypoparathyroidism. This brings us to understand that additionally, one of her sons also presented with similar intracerebral calcification, and was subsequently diagnosed with FD. Thus, her case was consistent with that of a patient experiencing FD. The patient had hypertension, which we now know might have caused the intracerebral hemorrhage. However, this patient's brain lesions were in uncommon locations for spontaneous intracerebral hemorrhage, and the lesions were noted as occurring away from the identified heavily calcified areas. Thus, it seemed that the massive calcification of cerebral vessels in the basal ganglia, the most common site of intracerebral hemorrhage, might have prevented a hypertensive intracerebral hemorrhage. Eventually, an intracerebral hemorrhage occurred in an uncommon location in the patient's brain.
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