Headache associated with moyamoya disease: a case story and literature review

Abstract

Headache associated with moyamoya disease (HAMD) is common in moyamoya disease. However, the characteristics and classification of HAMD are largely unknown. We present a case of a 39-year-old woman with HAMD. To characterize and classify the features of this syndrome, the patient was asked to complete a 4-month diagnostic headache diary. There was a total of 15 ictal days. All episodes were without aura. The headache was more commonly pressing (10/15), mild to moderate in severity (14/15), unchanged by physical activity (11/15), and associated with photophobia (10/15). The International Headache Society Classification was utilized to determine that eight episodes met criteria for probable migraine without aura, while seven episodes met criteria for probable frequent episodic tension-type headache. We identified four other case reports of HAMD with partial descriptions of the characteristics. When combined with our patient, the median age was 34 years old (range 6–49, SD 16). Four were female, while the patient with cluster headache was male. The median time from headache onset to diagnosis with moyamoya disease was 9.5 months (range 0–192, SD 88.0). Headaches were described as migraine with aura in two of five cases, hemiplegic migraine in one of five, and cluster headache in one of five. The highest intensity was described as severe in three of three cases, in which headache intensity was reported. Meanwhile, nausea, vomiting, and photophobia were present in two of three cases, where these features were reported, while nausea without vomiting was seen in one of three cases. In all five cases, patients had other neurological symptoms, such as paresis, seizures, visual disturbances, dysarthria, allodynia, ptosis, and unilateral restless leg syndrome. In conclusion, HAMD can present as migraine without aura. It can be the first presenting symptom of moyamoya disease. The headache features are not diagnostic; hence, early neurovascular imaging should be considered in patients with new onset, refractory migraine-like headache, especially in the setting of other neurological symptoms to exclude underlying moyamoya disease. Further reports using headache diaries are needed to better characterize HAMD as well as to determine whether headache with tension-type features is also part of this condition.

Moyamoya Disease Can Masquerade as Multiple Sclerosis

“…12 Headache is more common in MM, 13 and was an early symptom in more than half of our patients. The headaches in our patients resolved promptly after revascularization surgery, as is often the case, suggesting that in MM the headache is directly related to the vascular disease process.…”

Moyamoya in a Patient with Smith-Magenis Syndrome

“…Typical manifestations include weakness, numbness, speech changes, and seizures, as well as headaches and dizziness. To date, headaches and dizziness associated with moyamoya have not been well-characterized in the literature -and were not well-characterized in our patient -but headaches with migrainous and tension-like properties have been reported [23,24] .…”

Delayed posterior circulation insufficiency in pediatric moyamoya disease

“…Headache is a rather vague symptom presented in MMD patients in complex ways [16,20]. 'Preoperative' headache due to the ischemia of anterior circulation territory is not uncommon in initially diagnosed MMD patients, found in 20 * 30 % [20]. Various forms of headaches have been reported in MMD patients such as migraine-like headache with or without aura, and associated nausea and vomiting.…”

“…In other words, 'postoperative' headache occurring after effective improvement in the cerebral perfusion of the anterior circulation in MMD may be due to ischemia of the PCA territory. Headache is a rather vague symptom presented in MMD patients in complex ways [16,20]. 'Preoperative' headache due to the ischemia of anterior circulation territory is not uncommon in initially diagnosed MMD patients, found in 20 * 30 % [20].…”