WordNet
- a congenital bright red superficial vascular tumor resembling a strawberry; tends to decrease in size during childhood (同)strawberry haemangioma
- any of various low perennial herbs with many runners and bearing white flowers followed by edible fruits having many small achenes scattered on the surface of an enlarged red pulpy berry
- a soft red birthmark (同)strawberry_mark, hemangioma_simplex
- sweet fleshy red fruit
- benign angioma consisting of a mass of blood vessels; some appear as birthmarks (同)haemangioma
PrepTutorEJDIC
- 〈C〉『イチゴ』(イチゴ属の草の総称) / 〈C〉『イチゴの実』 / 〈U〉イチゴ色,深紅色
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/09/09 20:50:06」(JST)
[Wiki en表示]
| Capillary hemangioma |
| Classification and external resources |
A small hemangioma of infancy |
| ICD-10 |
D18.0,(ILDS D18.015) |
| ICD-9 |
757.32 |
| ICD-O: |
9131/0 |
| DiseasesDB |
30032 |
| eMedicine |
oph/691 |
| MeSH |
D018324 |
Strawberry naevus, H&E stain
A capillary hemangioma (also known as an "Infantile hemangioma,"[1] "Strawberry hemangioma"[2]:593, and "Strawberry nevus"[1]) is the most common variant of hemangioma which appears as a raised, red, lumpy area of flesh anywhere on the body, though 83% occur on the head or neck area.[3] These marks occur in about 10% of all births[4]:81, and usually appear between one and four weeks after birth.[5] It may grow rapidly, before stopping and slowly fading. Some are gone by the age of 2, about 60% by 5 years, and 90–95% by 9 years.[5] Capillary hemangioma is a vascular anomaly.
Capillary hemangiomas occur 5 times more often in female infants than in males, and mostly in Caucasian populations.[3][6] Additionally, low birthweight infants have a 26% chance of developing a hemangioma.[3][6]
It is the most common tumor of orbit and periorbital areas in childhood.It may occur in the skin,subcutaneous tissues and mucous membranes of oral cavities and lips as well as in the liver,spleen and kidneys. While this birthmark may be alarming in appearance, physicians generally counsel that it be left to disappear on its own, unless it is in the way of vision or blocking the nostrils.[5]
See also
- Hemangioma
- List of cutaneous conditions
References
- ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
- ^ a b c "Hemangioma Information". Vascular Birthmark Foundation. http://www.birthmark.org/hemangiomas.php. Retrieved 2008-08-02.
- ^ Sadler, Thomas W. (2009). Langman's Medical Embryology. (11th ed.). Lippincott Williams & Wilkins. ISBN 1-60547-656-0.
- ^ a b c "Birthmarks". Parenting and Child Health website. http://www.cyh.com/HealthTopics/HealthTopicDetails.aspx?p=114&np=304&id=1589. Retrieved 2008-08-02.
- ^ a b "Birthmarks". American Academy of Dermatology. http://www.aad.org/public/publications/pamphlets/common_vascular.html. Retrieved 2008-08-02.
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Vascular tissue neoplasm (ICD-O 9120–9179) (C49+C46/D18, 171+176/215)
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| Blood |
Hemangioma/hemangiosarcoma · Blue rubber bleb nevus syndrome · Hemangioendothelioma (Infantile hemangioendothelioma · Endovascular papillary hemangioendothelioma · Epithelioid hemangioendothelioma · Spindle cell hemangioendothelioma · Composite hemangioendothelioma · Proliferating angioendotheliomatosis · Retiform hemangioendothelioma) · Hemangiopericytoma · Capillary hemangioma (Hemangioblastoma) · Cavernous hemangioma · Venous lake
Kaposi's sarcoma: African cutaneous Kaposi sarcoma · African lymphadenopathic Kaposi sarcoma · AIDS-associated Kaposi sarcoma · Classic Kaposi sarcoma · Immunosuppression-associated Kaposi sarcoma · Kaposiform hemangioendothelioma
Angioma serpiginosum · Cherry angioma · Glomeruloid hemangioma · Microvenular hemangioma · Spider angioma · Targetoid hemosiderotic hemangioma · Tufted angioma · Universal angiomatosis
Angiokeratoma · Angiokeratoma of Mibelli · Angiolipoma
Pyogenic granuloma
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| Lymphatic |
Lymphangioma/lymphangiosarcoma · PEComa (Lymphangioleiomyomatosis) · Cystic hygroma · Lymphangioma circumscriptum
Multifocal lymphangioendotheliomatosis · Acquired progressive lymphangioma · Lymphangiomatosis
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| Either |
Angioma/angiosarcoma · Angiofibroma
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anat(a:h/u/t/a/l,v:h/u/t/a/l)/phys/devp/cell/prot
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noco/syva/cong/lyvd/tumr, sysi/epon, injr
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proc, drug(C2s+n/3/4/5/7/8/9)
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Congenital malformations and deformations of integument / skin disease (Q80–Q82, 757.0–757.3)
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| Genodermatosis |
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Congenital ichthyosis/
erythrokeratodermia
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AD
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Ichthyosis vulgaris
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AR
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Congenital ichthyosiform erythroderma: Epidermolytic hyperkeratosis · Lamellar ichthyosis (Harlequin type ichthyosis)
Netherton syndrome · Zunich–Kaye syndrome · Sjögren–Larsson syndrome
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XR
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X-linked ichthyosis
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Ungrouped
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Ichthyosis bullosa of Siemens · Ichthyosis follicularis · Ichthyosis prematurity syndrome · Ichthyosis–sclerosing cholangitis syndrome · Nonbullous congenital ichthyosiform erythroderma · Ichthyosis linearis circumflexa · Ichthyosis hystrix
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EB
and related
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EBS (EBS-K, EBS-WC, EBS-DM, EBS-OG, EBS-MD, EBS-MP)
JEB (JEB-H, Mitis, Generalized atrophic, JEB-PA)
DEB (DDEB, RDEB)
related: Costello syndrome · Kindler syndrome · Laryngoonychocutaneous syndrome · Skin fragility syndrome ·
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Ectodermal dysplasia
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Naegeli syndrome/Dermatopathia pigmentosa reticularis · Hay–Wells syndrome · Hypohidrotic ectodermal dysplasia · Focal dermal hypoplasia · Ellis–van Creveld syndrome · Rapp–Hodgkin syndrome/Hay–Wells syndrome
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Elastic/Connective
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Ehlers–Danlos syndrome · Cutis laxa (Gerodermia osteodysplastica) · Popliteal pterygium syndrome · Pseudoxanthoma elasticum · Van Der Woude syndrome
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Hyperkeratosis/
keratinopathy
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PPK
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diffuse: Diffuse epidermolytic palmoplantar keratoderma • Diffuse nonepidermolytic palmoplantar keratoderma • Palmoplantar keratoderma of Sybert • Mal de Meleda •
syndromic (connexin (Bart–Pumphrey syndrome • Clouston's hidrotic ectodermal dysplasia • Vohwinkel syndrome) • Corneodermatoosseous syndrome • plakoglobin (Naxos syndrome) • Scleroatrophic syndrome of Huriez • Olmsted syndrome • Cathepsin C (Papillon–Lefèvre syndrome • Haim–Munk syndrome) • Camisa disease
focal: Focal palmoplantar keratoderma with oral mucosal hyperkeratosis • Focal palmoplantar and gingival keratosis • Howel–Evans syndrome • Pachyonychia congenita (Pachyonychia congenita type I • Pachyonychia congenita type II) • Striate palmoplantar keratoderma • Tyrosinemia type II)
punctate: Acrokeratoelastoidosis of Costa • Focal acral hyperkeratosis • Keratosis punctata palmaris et plantaris • Keratosis punctata of the palmar creases • Schöpf–Schulz–Passarge syndrome • Porokeratosis plantaris discreta • Spiny keratoderma
ungrouped: Palmoplantar keratoderma and spastic paraplegia • desmoplakin (Carvajal syndrome) • connexin (Erythrokeratodermia variabilis • HID/KID)
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Other
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Meleda disease · Keratosis pilaris · ATP2A2 (Darier's disease) · Dyskeratosis congenita · Lelis syndrome
Dyskeratosis congenita · Keratolytic winter erythema · Keratosis follicularis spinulosa decalvans · Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome · Keratosis pilaris atrophicans faciei · Keratosis pilaris
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Other
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cadherin (EEM syndrome) · immune system (Hereditary lymphedema, Mastocytosis/Urticaria pigmentosa) · Hailey–Hailey
see also Template:Congenital malformations and deformations of skin appendages, Template:Phakomatoses, Template:Pigmentation disorders, Template:DNA replication and repair-deficiency disorder
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Developmental
anomalies |
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Midline
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Dermoid cyst · Encephalocele · Nasal glioma · PHACE association · Sinus pericranii
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Nevus
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Capillary hemangioma · Port-wine stain (Nevus flammeus nuchae)
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Other/ungrouped
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Aplasia cutis congenita · Amniotic band syndrome · Branchial cyst · Cavernous venous malformation
Accessory nail of the fifth toe · Bronchogenic cyst · Congenital cartilaginous rest of the neck · Congenital hypertrophy of the lateral fold of the hallux · Congenital lip pit · Congenital malformations of the dermatoglyphs · Congenital preauricular fistula · Congenital smooth muscle hamartoma · Cystic lymphatic malformation · Median raphe cyst · Melanotic neuroectodermal tumor of infancy · Mongolian spot · Nasolacrimal duct cyst · Omphalomesenteric duct cyst · Poland anomaly · Rapidly involuting congenital hemangioma · Rosenthal–Kloepfer syndrome · Skin dimple · Superficial lymphatic malformation · Thyroglossal duct cyst · Verrucous vascular malformation · Birthmark
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noco(i/b/d/q/u/r/p/m/k/v/f)/cong/tumr(n/e/d), sysi/epon
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proc, drug (D2/3/4/5/8/11)
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UpToDate Contents
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English Journal
- CHANDELIER-ASSISTED EXTERNAL DRAINAGE OF SUBRETINAL FLUID.
- Chhablani J1, Balakrishnan D.
- Retinal cases & brief reports.Retin Cases Brief Rep.2015 Mar 12. [Epub ahead of print]
- PURPOSE: External drainage could be indicated for long-standing nonresolving exudative retinal detachment secondary to chronic central serous chorioretinopathy, capillary hemangioma, and Coats disease. The authors report a modified technique of external drainage of subretinal fluid using Chandelier
- PMID 25767900
- Reticular infantile hemangiomas with minimal or arrested growth associated with lipoatrophy.
- Bessis D1, Bigorre M2, Labrèze C3.
- Journal of the American Academy of Dermatology.J Am Acad Dermatol.2015 Mar 9. pii: S0190-9622(15)00093-6. doi: 10.1016/j.jaad.2015.01.028. [Epub ahead of print]
- BACKGROUND: Reticular infantile hemangioma (RIH) with minimal or arrested growth (MAG) is an underrecognized variant of infantile hemangioma (IH).OBJECTIVE: We describe a new clinical subtype of RIH-MAG associated with lipoatrophy.METHODS: The medical charts and serial clinical photographs and imagi
- PMID 25766364
- Mesenteric cavernous hemangioma: Imaging-pathologic correlation.
- Si-Mohamed S1, Aufort S2, Khellaf L3, Ramos J3, Gasne P4, Durand L3.
- Diagnostic and interventional imaging.Diagn Interv Imaging.2015 Mar 5. pii: S2211-5684(15)00073-X. doi: 10.1016/j.diii.2015.01.006. [Epub ahead of print]
- PMID 25753543
Japanese Journal
- 乳児血管腫に対しプロプラノロール内服治療を行った4例
- 北村 弥生,橋本 一郎,石田 創士,高津 州雄,中西 秀樹
- 日形会誌 : 日本形成外科学会会誌 = Journal of Japan Society of Plastic and Reconstructive Surgery 33(8), 596-603, 2013-08-20
- NAID 10031194706
- 体幹に発生したRICH (rapidly involuting congenital hemangioma) の2例
- 石川 耕資,齋藤 典子,岩嵜 大輔,長尾 宗朝,佐々木 了
- 日形会誌 : 日本形成外科学会会誌 = Journal of Japan Society of Plastic and Reconstructive Surgery 32(11), 856-860, 2012-11-20
- NAID 10031129810
Related Links
- hemangioma /he·man·gi·o·ma/ (he-man″je-o´mah) 1. a benign tumor, usually in infants or children, made up of newly formed blood vessels and resulting from malformation of angioblastic tissue of fetal life. 2. a benign or malignant ...
- Strawberry Hemangioma (Infantile Hemangioma): A parent's guide for infants and babies - Overview. Hemangiomas are harmless tumors that are the result of rapidly dividing cells of the blood vessel walls, known as… ... ...
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イチゴ、イチゴ状の
- 関
- Fragaria