1.Multiple basal cell carcinoma associated with keratoacanthoma.
Sung Ku AHN ; Hyung Soon LEE ; Seung Kyung HAN ; Seung Hun LEE ; Sungnack LEE ; S K AHN ; H S LEE ; S K HAN ; S H LEE ; S LEE
Yonsei Medical Journal 1992;33(3):277-280
We report a case of multiple basal cell carcinoma associated with keratoacanthoma. A 65-year-old Korean female had suffered from multiple, variable-sized papules and nodules on the face for 20 years previous to treatment. She had no history of arsenic intake, irradiation, herb medication, or hereditable or preexisting dermatoses. Histopathologically, the tumors revealed typical findings of solid and adenoid types of basal cell carcinoma and keratoacanthoma.
Aged
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Carcinoma, Basal Cell/complications/*pathology
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Case Report
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Facial Neoplasms/complications/*pathology
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Female
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Human
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Keratoacanthoma/complications/*pathology
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Skin Neoplasms/complications/*pathology
2.Intracisternal Administration of Voltage Dependent Calcium Channel Blockers Attenuates Orofacial Inflammatory Nociceptive Behavior in Rats.
Kyoung A WON ; Sang H PARK ; Bo K KIM ; Kyoung S BAEK ; Dong H YOON ; Dong K AHN
International Journal of Oral Biology 2011;36(2):43-50
Voltage dependent calcium channel (VDCC), one of the most important regulator of Ca2+ concentration in neuron, play an essential role in the central processing of nociceptive information. The present study investigated the antinociceptive effects of L, T or N type VDCC blockers on the formalin-induced orofacial inflammatory pain. Experiments were carried out on adult male Sprague-Dawley rats weighing 220-280 g. Anesthetized rats were individually fixed on a stereotaxic frame and a polyethylene (PE) tube was implanted for intracisternal injection. After 72 hours, 5% formalin (50 microL) was applied subcutaneously to the vibrissa pad and nociceptive scratching behavior was recorded for nine successive 5 min intervals. VDCC blockers were administered intracisternally 20 minutes prior to subcutaneous injection of formalin into the orofacial area. The intracisternal administration of 350 or 700 microg of verapamil, a blocker of L type VDCC, significantly decreased the number of scratches and duration in the behavioral responses produced by formalin injection. Intracisternal administration of 75 or 150 microg of mibefradil, a T type VDCC blocker, or 11 or 22 microg of cilnidipine, a N type VDCC blocker, also produced significant suppression of the number of scratches and duration of scratching in the first and second phase. Neither intracisternal administration of all VDCC blockers nor vehicle did not affect in motor dysfunction. The present results suggest that central VDCCs play an important role in orofacial nociceptive transmission and a targeted inhibition of the VDCCs is a potentially important treatment approach for inflammatory pain originating in the orofacial area.
Adult
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Animals
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Calcium
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Calcium Channel Blockers
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Calcium Channels
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Calcium Channels, L-Type
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Calcium Channels, N-Type
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Calcium Channels, T-Type
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Dihydropyridines
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Facial Pain
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Formaldehyde
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Humans
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Injections, Subcutaneous
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Male
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Mibefradil
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Neurons
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Pain Measurement
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Polyethylene
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Rats
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Rats, Sprague-Dawley
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Verapamil
3.Glia Dose not Participate in Antinociceptive Effects of Gabapentin in Rats with Trigeminal Neuropathic Pain.
Kui Y YANG ; Hak K KIM ; Myoung U JIN ; Jin S JU ; Dong K AHN
International Journal of Oral Biology 2012;37(3):121-129
Previous clinical studies have demonstrated that gabapentin, a drug that binds to the voltage-gated calcium channel alpha2delta1 subunit proteins, is effective in the management of neuropathic pain, but there is limited evidence that addresses the participation of glial cells in the anti-allodynic effects of this drug. The present study investigated the participation of glial cells in the anti-nociceptive effects of gabapentin in rats with trigeminal neuropathic pain produced by mal-positioned dental implants. Under anesthesia, the left mandibular second molar was extracted and replaced by a miniature dental implant to induce injury to the inferior alveolar nerve. Mal-positioned dental implants significantly decreased the air-puff thresholds both ipsilateral and contralateral to the injury site. Gabapentin was administered intracisternally beginning on postoperative day (POD) 1 or on POD 7 for three days. Early or late treatment with 0.3, 3, or 30 microg of gabapentin produced significant anti-allodynic effect in the rats with mal-positioned dental implants. On POD 9, in the mal-positioned dental implants group, OX-42, a microglia marker, and GFAP, an astrocyte marker, were found to be up-regulated in the medullary dorsal horn, compared with the naive group. However, the intracisternal administration of gabapentin (30 microg) failed to reduce the number of activated microglia or astrocytes in the medullary dorsal horn. These findings suggest that gabapentin produces significant anti-nociceptive effects, which are not mediated by the inhibition of glial cell function in the medullary dorsal horn, in a rat model of trigeminal neuropathic pain.
Amines
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Anesthesia
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Animals
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Astrocytes
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Calcium Channels
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Cyclohexanecarboxylic Acids
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Dental Implants
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gamma-Aminobutyric Acid
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Horns
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Mandibular Nerve
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Microglia
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Molar
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Neuralgia
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Neuroglia
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Proteins
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Rats