Recurrent trigeminal neuralgia caused by an anomalous cerebellar artery arising from the persistent primitive trigeminal artery: illustrative case.
- 1Department of Neurosurgery, Kameda Medical Center, Kamogawa, Chiba.
- 2Department of Neurosurgery, Jikei University School of Medicine, Minato-ku, Tokyo, Japan.
Abstract
Background
Persistent primitive trigeminal artery (PTA) and its related variants-the PTA family-are rare vascular anomalies that can cause trigeminal neuralgia through atypical neurovascular compression patterns, requiring careful anatomical evaluation. The authors describe a rare case of recurrent trigeminal neuralgia caused by an anomalous cerebellar artery arising from a PTA and further complicated by a long-standing Teflon granuloma.Observations
A 79-year-old man developed recurrent trigeminal neuralgia 19 years after microvascular decompression. Imaging revealed an anomalous anterior inferior cerebellar artery (AICA) arising from a PTA and compressing the trigeminal nerve, along with a Teflon granuloma obscuring the vessel's course. Three-dimensional multimodal reconstruction clarified the neurovascular conflict. During surgery, dense adhesions due to the granuloma were encountered, and maximal granuloma removal enabled successful transposition of the anomalous AICA.Lessons
PTA family anomalies can produce trigeminal neuralgia through atypical patterns of neurovascular compression. In complex or recurrent cases, preoperative 3D reconstruction imaging can enhance understanding of aberrant vascular anatomy. Maximal safe removal of a Teflon granuloma is crucial to create sufficient space and facilitate adequate decompression of the offending vessel. https://thejns.org/doi/10.3171/CASE2699.
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BibTeX
@article{narita2026recurrent,
title = {{Recurrent trigeminal neuralgia caused by an anomalous cerebellar artery arising from the persistent primitive trigeminal artery: illustrative case.}},
author = {Hiroki Narita and Nobuyuki Watanabe and Kentaro Watanabe and Ryoto Wachi and Kohei Ishikawa and Michihiro Tanaka and Yuichi Murayama},
journal = {Journal of neurosurgery. Case lessons},
year = {2026},
month = oct,
doi = {10.3171/case2699},
url = {https://europepmc.org/article/MED/42896238},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Recurrent trigeminal neuralgia caused by an anomalous cerebellar artery arising from the persistent primitive trigeminal artery: illustrative case.
AU - Hiroki Narita
AU - Nobuyuki Watanabe
AU - Kentaro Watanabe
AU - Ryoto Wachi
AU - Kohei Ishikawa
AU - Michihiro Tanaka
AU - Yuichi Murayama
PY - 2026
DA - 2026/10/19
JO - Journal of neurosurgery. Case lessons
DO - 10.3171/case2699
UR - https://europepmc.org/article/MED/42896238
AB - Background Persistent primitive trigeminal artery (PTA) and its related variants-the PTA family-are rare vascular anomalies that can cause trigeminal neuralgia through atypical neurovascular compression patterns, requiring careful anatomical evaluation. The authors describe a rare case of recurrent trigeminal neuralgia caused by an anomalous cerebellar artery arising from a PTA and further complicated by a long-standing Teflon granuloma.Observations A 79-year-old man developed recurrent trigeminal neuralgia 19 years after microvascular decompression. Imaging revealed an anomalous anterior inferior cerebellar artery (AICA) arising from a PTA and compressing the trigeminal nerve, along with a Teflon granuloma obscuring the vessel's course. Three-dimensional multimodal reconstruction clarified the neurovascular conflict. During surgery, dense adhesions due to the granuloma were encountered, and maximal granuloma removal enabled successful transposition of the anomalous AICA.Lessons PTA family anomalies can produce trigeminal neuralgia through atypical patterns of neurovascular compression. In complex or recurrent cases, preoperative 3D reconstruction imaging can enhance understanding of aberrant vascular anatomy. Maximal safe removal of a Teflon granuloma is crucial to create sufficient space and facilitate adequate decompression of the offending vessel. https://thejns.org/doi/10.3171/CASE2699.
SN - 2694-1902
ER -