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Cephalgia Alopecia
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Purpose of review: In this review, we examine reported cases of cephalgia alopecia including the initial case report from 2006. The goal is to review the clinical description, pathophysiology, diagnosis, and treatment of cephalgia
Alopecia areata and homolateral headache due to an impacted superior wisdom tooth.
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A case of alopecia areata and homolateral headache due to an impacted superior wisdom tooth is reported. After the extraction, the headache disappeared, hair regrew in the alopecic area and in 4 months completely covered the whole area.
Cephalalgia alopecia or nummular headache with trophic changes? A new case with prolonged follow-up.
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Cephalalgia alopecia is a rare and recently described headache syndrome in which recurrent, burning head and neck pain is associated with hair loss from areas of scalp affected by the pain. We here report the case of a 33-year-old woman with continuous unilateral occipital pain and colocalized
Alopecia and cutis verticis gyrata due to traction presenting as headache.
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31-year-old woman with chronic daily headache and alopecia.
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Cephalalgic alopecia areata: a syndrome of neuralgiform head pain and hair loss responsive to botulinum A toxin injection.
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Botulinum toxin treatment of cephalalgia alopecia increases substance P and calcitonin gene-related peptide-containing cutaneous nerves in scalp.
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Botulinum toxin treatment of secondary headaches and cranial neuralgias: a review of evidence.
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BACKGROUND
Recent scientific data support an effect of botulinum neurotoxin (BoNT) on pain and headache.
OBJECTIVE
We sought to conduct a systematic review of BoNT in the secondary headaches and cranial neuralgias.
METHODS
MEDLINE, EMBASE, Cochrane, ClinicalTrials.gov and reference lists were
Alopecia areata treated with hydroxychloroquine: A retrospective study of nine pediatric cases.
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OBJECTIVE
Alopecia areata is a common hair loss condition that is often emotionally devastating for patients. There is a paucity of effective treatments available. Hydroxychloroquine has been reported as variably effective in inducing significant hair regrowth in adults with alopecia areata. The
Diphenylcyclopropenone in patients with alopecia areata. A critically appraised topic.
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OBJECTIVE
To assess the efficacy and safety of topical diphenylcyclopropenone (DPCP) in patients with alopecia areata.
METHODS
Study selection, data extraction, risk of bias assessment and analyses were carried out independently by two authors. The quality of evidence was rated with Grading of
Scalp cooling for hair loss prevention in female Japanese breast cancer patients receiving (neo)adjuvant chemotherapy.
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5 mg/day finasteride treatment for normoandrogenic Asian women with female pattern hair loss.
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BACKGROUND
Various treatments have been attempted for female pattern hair loss (FPHL), including topical minoxidil, oral antiandrogen and finasteride. But, there is no consensus on the standard treatment options. Clinical efficacy of finasteride in treating FPHL is still in controversy, but there is
[Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].
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We report a 52-year-old man with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) presenting dementia, alopecia and lumbar herniated disk. He had an episode of stroke and migraine-like headache lasting for 5 minutes. A lot of members had cerebral
Treatment of widespread alopecia areata in young patients with monthly oral corticosteroid pulse.
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Sixteen patients up to 18 years of age with widespread alopecia areata (AA) were recruited for the study. They included 10 patients with extensive AA (> or = 40% loss of scalp hair and or more than 10 patches scattered over the scalp and body) and 3 each with alopecia totalis and circumscribed
Headache and bilateral visual loss in a young hypothyroid Indian man.
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We describe the exceptional association of Vogt-Koyanagi-Harada syndrome (VKHS) and hypothyroidism in a 29-year-old man of Indian heritage. VKHS is a rare uveomeningoencephalitic syndrome with probably autoimmune pathogenesis. Nontraumatic uveitis, aseptic meningoencephalitis, vitiligo, alopecia and
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