A systematic review on persistent trigeminal artery, in searching for a therapeutic solution to idiopathic and unresponsive trigeminal nerve inflammations and migraines.

B-nicotinamide adenine dinucleotide (NADH) CT-angiography estrogen human placenta extract (HPE) migraine-cephalgia persistent trigeminal artery progesterone testosterone trigeminal nerve

Journal

Journal of biological regulators and homeostatic agents
ISSN: 0393-974X
Titre abrégé: J Biol Regul Homeost Agents
Pays: Italy
ID NLM: 8809253

Informations de publication

Date de publication:
Historique:
entrez: 20 5 2020
pubmed: 20 5 2020
medline: 1 7 2020
Statut: ppublish

Résumé

The rarely diagnosed persistent trigeminal artery (PTA) originates from the posterior bend or lateral wall of the intracavernous carotid artery and is the most common occurring type of remnant primitive fetal arteries. Even if PTA is uncommon, information and awareness about it could be of great help for clinicians dealing with cranial vascular imaging and operating this region. In addition, it could give a supporting response to the presence of a wide range of idiopathic and unresponsive disturbs that sometimes are erroneously interpreted and treated. There are very few published scientific reports of coexisting PTA and unilateral trigeminal neuralgia and migraine-cephalgia (MC). In this review we describe few reported and unreported cases regarding the manifestation of unresponsive trigeminal neuralgia and migraine due to the presence of PTA. Patients usually present with a clinical symptomatology with unstable blood hypertension, pain of typical trigeminal neuralgia and MC that cover unilaterally the occipital area over the second and third divisions of the nerve. The outbreaks may often become more severe during physical exertion, stress and hypertension. Angio-MRI may reveal the PTA with an occasional occurrence of parietal cavernoma. We also describe a case of chronic left MC case associated with an adjacent PTA close to the trigeminal nerve position. The size and location of the PTA was confirmed by a CT-Angiography. The MC was safely treated by bio-identical testosterone, human placenta extract (HPE), b-nicotinamide adenine dinucleotide (NADH) and low dose amlopidine. It is hypothesized that these types of primitive anastomose arteries that fully belong to the intracranial arterial vascular system do not perform any supportive functional activity. Nevertheless, they undergo the normal biological decay caused by the aging process and metabolic dysfunctions. Therefore, such primitive fetal arteries as PTA might be subjected not only to a faster structural deterioration but they would actively contribute to a series of mechanisms causing a variety of idiopathic intracranial vascular and structural symptoms. Consequently, this would change the primary therapeutic approach to solve this problem, today represented by surgical removal. Anatomic implications related to treatment procedure are also discussed.

Identifiants

pubmed: 32425036
pii: 18

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-169. DENTAL SUPPLEMENT

Informations de copyright

Copyright 2020 Biolife Sas. www.biolifesas.org.

Auteurs

C Gargiulo Isacco (C)

Department of Interdisciplinary Medicine (D.I.M.), the School of Medicine, University of Bari "Aldo Moro".
Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari Aldo Moro, Italy.

A Ballini (A)

Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari Aldo Moro, Italy.

G Paduanelli (G)

Department of Interdisciplinary Medicine (D.I.M.), the School of Medicine, University of Bari "Aldo Moro".

K C D Nguyen (KCD)

Department of Interdisciplinary Medicine (D.I.M.), University of Bari Aldo Moro, Italy.

M Schiffman (M)

Plastic Surgeon Consultant.

S K Aityan (SK)

Professor and Director of Multidisciplinary Research Center, Oakland, California, USA.

O Tapparo (O)

University of Medicine, Hermannstadt City, Germany.

N Khoa (N)

Nhan Tham International Odonto-Stomatology Clinic, Ho Chi Minh City, Vietnam.

G Dipalma (G)

Department of Interdisciplinary Medicine (D.I.M.), University of Bari Aldo Moro, Italy.

F Inchingolo (F)

Department of Interdisciplinary Medicine (D.I.M.), University of Bari Aldo Moro, Italy.

T C Tran (TC)

Pham Ngoc Thac University of Medicine, Department of Histology, Embryology and Genetics, Ho Chi Minh City, Vietnam.

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