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DOI 10.1007/s00701-015-2422-8

Медицинская библиотека · Acta neurochirurgica · 2015

Moyamoya disease concurrent with Graves' disease treated by direct bypass: clinical features and treatment strategies.

Ryu Bikei, Kawamata Takakazu, Yamaguchi Koji, Kawashima Akitsugu, Ono Masami, Okada Yoshikazu

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Аннотация

BACKGROUND

Moyamoya disease (MMD) concurrent with Graves' disease (GD) is rare. There is no guideline about optimizing thyroid hormones and the appropriate timing of surgical treatment for MMD with GD.

METHODS

We encountered eight patients with MMD and GD presenting with cerebral ischemia who were treated by direct bypass. Thyroid hormones [free thyroxin (fT4) and free triiodothyronine (fT3)], thyroid-stimulating hormone (TSH), and TSH receptor antibody (TRAb) were measured sequentially. After thyrotoxic conditions were medically optimized, revascularization surgery was performed by superficial temporal artery-middle cerebral artery (STA-MCA) double bypass in all cases. Clinical outcomes were estimated by modified Rankin scale (mRS) at discharge and 3 months after surgery.

RESULTS

In six patients with thyrotoxicosis, the fT4, fT3, and TRAb (range) at the onset of cerebral ischemia were 4.81-10.30 pg/ml, 13.08-31.90 pg/ml, and 3.5-83.8 IU/l, respectively. At surgery, mean (range) fT3 and fT4 were optimized to 3.02 (1.01-4.87) pg/ml and 1.09 (0.41-1.68) ng/dl, respectively. In the thyrotoxic cases, it took 70-310 days (mean, 142 days) to optimize thyroid hormones before surgery. There was no neurological aggravation after surgery, and outcome was excellent at 3 months with mRS scores ≤2 in all cases.

CONCLUSIONS

For MMD concurrent with GD, optimizing thyroid hormones followed by STA-MCA double bypass was successful to prevent cerebral ischemic events.

Для цитирования: Ryu Bikei, Kawamata Takakazu, Yamaguchi Koji, Kawashima Akitsugu, Ono Masami, Okada Yoshikazu. Moyamoya disease concurrent with Graves' disease treated by direct bypass: clinical features and treatment strategies.. Acta neurochirurgica. 2015. DOI: 10.1007/s00701-015-2422-8.

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