WordNet
- criticize harshly, usually via an electronic medium; "the person who posted an inflammatory message got flamed"
- be in flames or aflame; "The sky seemed to flame in the Hawaiian sunset"
PrepTutorEJDIC
- 〈U〉〈C〉《しばしば複数形で》『炎』 / 〈U〉炎のような輝き;炎色 / 〈C〉《おもに文》(…の)(燃えるような)情熱,激情《+『of』+『名』》 / 『炎をあげて燃える』,燃えさかる《+『up』》 / (炎のように)照え映える《+『up』》 / 〈怒り・情熱などが〉燃え上がる;〈人が〉かっと怒り出す《+『out』(『up, forth』)》
- 燃えている / 光り輝く;燃えるように赤い;焼けつくような / (人が)情熱に燃える;(感情が)熱烈な
- 母斑(ぼはん)(先天性のあざ・ほくろ・そばかすなど)
UpToDate Contents
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- 1. 新生児および乳児における皮膚および頭皮の良性病変 benign skin and scalp lesions in the newborn and young infant
- 2. 色素沈着過剰を有する患者へのアプローチ approach to the patient with hyperpigmentation disorders
- 3. 色素細胞性母斑（ほくろ）以外の良性色素性皮膚病変 benign pigmented skin lesions other than melanocytic nevi moles
- 4. 非定型母斑（異形成母斑） atypical dysplastic nevi
- 5. 後天性色素性母斑（ほくろ） acquired melanocytic nevi moles
English Journal
- [Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years].
- Rupprecht M1, Mensing CH, Barvencik F, Ittrich H, Heiland M, Rueger JM, Amling M, Pogoda P.
- RöFo : Fortschritte auf dem Gebiete der Röntgenstrahlen und der Nuklearmedizin.Rofo.2007 Jun;179(6):618-26. Epub 2007 May 9.
- PURPOSE: In 1960 Gorlin and Goltz defined the nevoid basal cell carcinoma syndrome (NBCCS, Gorlin-Goltz Syndrome) as a syndrome comprising multiple basal cell carcinoma, odontogenic keratocysts, and skeletal anomalies. NBCCS is an autosomal dominantly inherited disease with an estimated prevalence o
- PMID 17492539
- Radiological features in 82 patients with nevoid basal cell carcinoma (NBCC or Gorlin) syndrome.
- Kimonis VE1, Mehta SG, Digiovanna JJ, Bale SJ, Pastakia B.
- Genetics in medicine : official journal of the American College of Medical Genetics.Genet Med.2004 Nov-Dec;6(6):495-502.
- PURPOSE: Nevoid Basal Cell Carcinoma Syndrome (NBCCS) is an autosomal-dominant disorder characterized by multiple basal cell carcinomas, jaw cysts, palmar/plantar pits, calcification of the falx cerebri, and spine and rib anomalies. NBCCS is due to mutations in PTCH1, the human homologue of the Dros
- PMID 15545745
- Conductive hearing loss in Beckwith-Wiedemann syndrome.
- Schick B1, Brors D, Prescher A, Draf W.
- International journal of pediatric otorhinolaryngology.Int J Pediatr Otorhinolaryngol.1999 May 5;48(2):175-9.
- Beckwith-Wiedemann syndrome is a rare genetic overgrowth syndrome presenting with organomegaly, abdominal wall defects, macroglossia, and postnatal hypoglycemia. Head and neck manifestations of this abnormality include flame nevus of the forehead and characteristic sulci of the ear lobe. We present
- PMID 10375044
Japanese Journal
- EMG syndromeの姉弟
- 先天異常 : 日本先天異常学会会報 : official journal of Congeital Anomalies Research Association of Japan 16(3), 163-167, 1976-09-30
- NAID 110002753880
Related Links
- nevus [ne´vus] (pl. ne´vi) (L.) a circumscribed stable malformation of the skin or sometimes the oral mucosa, which is not due to external causes; the excess (or deficiency) of tissue may involve epidermal, connective tissue, adnexal ...
- Thesaurus Antonyms Related Words Synonyms Legend: Switch to new thesaurus Noun 1. nevus flammeus - a flat birthmark varying from pink to purple port-wine stain birthmark, nevus - a blemish on the skin that is formed before ...
Related Pictures
★リンクテーブル★
| リンク元 | 「単純性血管腫」「焔状母斑」「火焔状母斑」 |
| 関連記事 | 「flame」 |
「単純性血管腫」
- ラ
- hemangioma simplex
- 同
- ポートワイン様血管腫、ポートワイン母斑 portwine stain portwine mark、火炎状母斑 焔状母斑 flame nevus naevus flammeus、成熟毛細血管腫 mature capillary angioma
- 関
- 血管腫
- 出生時より存在する表在性(真皮内)の毛細血管系異常であり、隆起しない紅斑を呈する。
病型
特殊な病型
治療
- 色素レーザー治療
予後
- サモンパッチ以外は自然消退しない
臨床関連
- 症候群の部分症となることがある
- スタージ-ウェーバー症候群 Sturge-Weber症候群
- クリッペル-トレノネー-ウェーバー症候群 Klippel-Trenaunary-Weber症候群
「焔状母斑」
- 英
- nevus flammeus、flame nevus
- 関
- 火炎状母斑、・ートワイン母斑
「火焔状母斑」
「flame」
- 関
- -itis