Nevoid hypertrichosis: Difference between revisions
Content deleted Content added
No edit summary |
Citation bot (talk | contribs) Add: pmc, pages. Removed parameters. | Use this bot. Report bugs. | Suggested by CursedWithTheAbilityToDoTheMath | #UCB_toolbar |
||
| (2 intermediate revisions by 2 users not shown) | |||
| Line 1: | Line 1: | ||
{{Infobox medical condition (new) |
{{Infobox medical condition (new) |
||
| name = <!--{{PAGENAME}} by default--> |
| name = <!--{{PAGENAME}} by default--> |
||
| synonym = |
| synonym = Hair nevus |
||
| image = |
| image = |
||
| image_size = |
| image_size = |
||
| Line 7: | Line 7: | ||
| caption = |
| caption = |
||
| pronounce = |
| pronounce = |
||
| specialty = |
| specialty = [[Dermatology]] |
||
| symptoms = |
| symptoms = |
||
| complications = |
| complications = |
||
| Line 24: | Line 24: | ||
| deaths = |
| deaths = |
||
}} |
}} |
||
'''Nevoid hypertrichosis''' is a cutaneous condition characterized by the growth of terminal hairs in a circumscribed area.<ref name="Bolognia">{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }}</ref> |
'''Nevoid hypertrichosis''' is a cutaneous condition characterized by the growth of [[Terminal hair|terminal hairs]] in a circumscribed area.<ref name="Bolognia">{{cite book |author=Rapini, Ronald P. |author2=Bolognia, Jean L. |author3=Jorizzo, Joseph L. |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }}</ref> Nevoid hypertrichosis often presents shortly after birth. The cause of nevoid hypertrichosis is unknown. The diagnosis is made based of clinical and histopathological examination. |
||
== Signs and symptoms == |
|||
Nevoid hypertrichosis is a rare disorder characterized by a confined patch of coarse [[terminal hair]].<ref name="pre-adolescent girl">{{cite journal | last1=Grover | first1=Chander | last2=Daulatabad | first2=Deepashree | last3=Tanveer | first3=Nadeem | title=Nevoid hypertrichosis in a pre-adolescent girl | journal=Indian Dermatology Online Journal | publisher=Medknow | volume=8 | issue=2 | year=2017 | pages=143–145 | issn=2229-5178 | doi=10.4103/2229-5178.202285 | doi-access=free | pmid=28405561 | pmc=5372441 }}</ref> It often manifests at or shortly after birth,<ref name="Iranian Girl">{{cite journal | last1=Vergani | first1=Raffaella | last2=Betti | first2=Roberto | last3=Martino | first3=Patrizia | last4=Crosti | first4=Carlo | title=Giant Nevoid Hypertrichosis in an Iranian Girl | journal=Pediatric Dermatology | publisher=Wiley | volume=19 | issue=1 | year=2002 | issn=0736-8046 | doi=10.1046/j.1525-1470.2002.01970.x | pages=64–66| pmid=11860575 }}</ref> while it sporadically manifests later in life.<ref name="Multiple">{{cite journal | last1=Chang | first1=Sung Nam | last2=Hong | first2=Chang Eui | last3=Kim | first3=Dong-Kun | last4=Park | first4=Wook Hwa | title=A Case of Multiple Nevoid Hypertrichosis | journal=The Journal of Dermatology | publisher=Wiley | volume=24 | issue=5 | year=1997 | issn=0385-2407 | doi=10.1111/j.1346-8138.1997.tb02801.x | pages=337–341| pmid=9198325 }}</ref> The lesion is known to stay stable, and the child's growth is directly correlated with any size rise.<ref name="pre-adolescent girl"/> Though reports of spontaneous resolution are rare, it usually persists.<ref name="spontaneous resolution">{{cite journal | last1=TE | first1=Dudding | last2=M | first2=Rogers | last3=LG | first3=Roddick | last4=J | first4=Relic | last5=MJ | first5=Edwards | title=Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution | journal=American Journal of Medical Genetics | date=1998 | publisher=Am J Med Genet | volume=79 | issue=3 | pages=195–196 | issn=0148-7299 | pmid=9788560 | doi=10.1002/(sici)1096-8628(19980923)79:3<195::aid-ajmg8>3.0.co;2-m |url=https://pubmed.ncbi.nlm.nih.gov/9788560/ | access-date=2024-04-23 }}</ref> It typically manifests as one or more isolated patches.<ref name="Multiple"/> |
|||
The absence of any underlying pigmentary alteration or other lesions is the traditional unifying characteristic of these lesions.<ref name="pre-adolescent girl"/> The hair in the lesions is the same color as the hair on the scalp; nevertheless, there have been instances of premature graying of the hair in the patch as well as depigmented hair.<ref name="Multiple"/> |
|||
== Causes == |
|||
Whether nevoid hypertrichosis is a genetically determined condition or a deformity of unknown etiology remains unclear.<ref name="review of the literature">{{cite journal | last1=Gupta | first1=Lipy | last2=Bharadwaj | first2=Minakshi | last3=Gautam | first3=RamKishan | title=Nevoid hypertrichosis: Case report with review of the literature | journal=International Journal of Trichology | publisher=Medknow | volume=3 | issue=2 | year=2011 | pages=115–117 | issn=0974-7753 | doi=10.4103/0974-7753.90829 | doi-access=free | pmid=22223975 | pmc=3250008 }}</ref> In giant nevoid hypertrichosis, an autosomal dominant pattern of inheritance has been suggested.<ref name="Iranian Girl"/> |
|||
== Diagnosis == |
|||
Histopathological analysis and traditional cutaneous appearance serve as the foundation for the diagnosis.<ref name="pre-adolescent girl"/> Histopathology is usually required to rule out any underlying [[nevus]], but it typically reveals a normal [[epidermis]] with an increased number of morphologically normal [[Hair follicle|hair follicles]] in the [[dermis]].<ref name="spontaneous resolution"/> |
|||
Congenital hairy [[melanocytic nevus]], congenital [[Hypertrichosis lanuginosa|hypertichosis lanuginosa]], [[plexiform neurofibroma]], and generalized [[hypertrichosis]] are differential diagnoses that need to be ruled out in cases with early onset. [[Becker's nevus]], late onset [[melanocytic nevus]], and smooth muscle [[hamartoma]] should be taken into consideration for patients with a delayed onset.<ref name="pre-adolescent girl"/> |
|||
== Treatment == |
|||
For management, the patient should be counseled about the condition's benign nature, which will relieve their anxieties. The goal of treatment is to improve appearance, particularly if the lesion is on a body part that is visible.<ref name="pre-adolescent girl"/> Long pulsed neodymium-doped yttrium aluminum garnet and [[alexandrite]] lasers have been tried for laser hair reduction with positive cosmetic results.<ref name="hair removal">{{cite journal | last1=Koch | first1=D. | last2=Pratsou | first2=P. | last3=Szczecinska | first3=W. | last4=Lanigan | first4=S. | last5=Abdullah | first5=A. | title=The diverse application of laser hair removal therapy: a tertiary laser unit's experience with less common indications and a literature overview | journal=Lasers in Medical Science | publisher=Springer Science and Business Media LLC | volume=30 | issue=1 | date=2013-10-31 | issn=0268-8921 | doi=10.1007/s10103-013-1464-5 | pages=453–467| pmid=24173910 }}</ref> |
|||
== See also == |
== See also == |
||
| Line 33: | Line 49: | ||
{{reflist}} |
{{reflist}} |
||
== Further reading == |
|||
| ⚫ | |||
* {{cite journal | last1=Sotiriadis | first1=Dimitrios | last2=Patsatsi | first2=Aikaterini | last3=Lazaridou | first3=Elizabeth | last4=Sotiriou | first4=Eleni | last5=Devliotou-Panagiotidou | first5=Despina | title=Multiple Nevoid Hypertrichosis as An Isolated Developmental Defect | journal=Pediatric Dermatology | publisher=Wiley | volume=26 | issue=4 | year=2009 | issn=0736-8046 | doi=10.1111/j.1525-1470.2009.00948.x | pages=436–438 | pmid=19689520 | ref=none}} |
|||
* {{cite journal | last1=Cox | first1=N.H. | last2=McCLURE | first2=J.P. | last3=Hardie | first3=R.A. | title=Naevoid hypertrichosis-report of a patient with multiple lesions | journal=Clinical and Experimental Dermatology | volume=14 | issue=1 | date=1989 | issn=0307-6938 | doi=10.1111/j.1365-2230.1989.tb00887.x | pages=62–64 | pmid=2805390 | ref=none}} |
|||
== External links == |
|||
* [https://dermnetnz.org/topics/hypertrichosis Hypertrichosis] - [[DermNet]] |
|||
{{Medical resources |
|||
{{Skin-appendage-stub|}} |
|||
| ICD11 = {{ICD11|LC30}} |
|||
| ICD10 = {{ICD10|L68.8}} |
|||
| ICD10CM = <!-- {{ICD10CM|Xxx.xxxx}} --> |
|||
| ICD9 = <!-- {{ICD9|xxx}} --> |
|||
| ICDO = |
|||
| OMIM = |
|||
| MeshID = |
|||
| DiseasesDB = |
|||
| SNOMED CT = 201161009 |
|||
| Curlie = |
|||
| MedlinePlus = |
|||
| eMedicineSubj = |
|||
| eMedicineTopic = |
|||
| PatientUK = |
|||
| NCI = |
|||
| GeneReviewsNBK = |
|||
| GeneReviewsName = |
|||
| NORD = |
|||
| GARDNum = |
|||
| GARDName = |
|||
| RP = |
|||
| AO = |
|||
| WO = |
|||
| OrthoInfo = |
|||
| Orphanet = |
|||
| Scholia = Q7004995 |
|||
| OB = |
|||
}} |
|||
{{Disorders of skin appendages}} |
|||
| ⚫ | |||
Latest revision as of 06:16, 23 April 2024
| Nevoid hypertrichosis | |
|---|---|
| Other names | Hair nevus |
| Specialty | Dermatology |
Nevoid hypertrichosis is a cutaneous condition characterized by the growth of terminal hairs in a circumscribed area.[1] Nevoid hypertrichosis often presents shortly after birth. The cause of nevoid hypertrichosis is unknown. The diagnosis is made based of clinical and histopathological examination.
Signs and symptoms
[edit]Nevoid hypertrichosis is a rare disorder characterized by a confined patch of coarse terminal hair.[2] It often manifests at or shortly after birth,[3] while it sporadically manifests later in life.[4] The lesion is known to stay stable, and the child's growth is directly correlated with any size rise.[2] Though reports of spontaneous resolution are rare, it usually persists.[5] It typically manifests as one or more isolated patches.[4]
The absence of any underlying pigmentary alteration or other lesions is the traditional unifying characteristic of these lesions.[2] The hair in the lesions is the same color as the hair on the scalp; nevertheless, there have been instances of premature graying of the hair in the patch as well as depigmented hair.[4]
Causes
[edit]Whether nevoid hypertrichosis is a genetically determined condition or a deformity of unknown etiology remains unclear.[6] In giant nevoid hypertrichosis, an autosomal dominant pattern of inheritance has been suggested.[3]
Diagnosis
[edit]Histopathological analysis and traditional cutaneous appearance serve as the foundation for the diagnosis.[2] Histopathology is usually required to rule out any underlying nevus, but it typically reveals a normal epidermis with an increased number of morphologically normal hair follicles in the dermis.[5]
Congenital hairy melanocytic nevus, congenital hypertichosis lanuginosa, plexiform neurofibroma, and generalized hypertrichosis are differential diagnoses that need to be ruled out in cases with early onset. Becker's nevus, late onset melanocytic nevus, and smooth muscle hamartoma should be taken into consideration for patients with a delayed onset.[2]
Treatment
[edit]For management, the patient should be counseled about the condition's benign nature, which will relieve their anxieties. The goal of treatment is to improve appearance, particularly if the lesion is on a body part that is visible.[2] Long pulsed neodymium-doped yttrium aluminum garnet and alexandrite lasers have been tried for laser hair reduction with positive cosmetic results.[7]
See also
[edit]References
[edit]- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ a b c d e f Grover, Chander; Daulatabad, Deepashree; Tanveer, Nadeem (2017). "Nevoid hypertrichosis in a pre-adolescent girl". Indian Dermatology Online Journal. 8 (2). Medknow: 143–145. doi:10.4103/2229-5178.202285. ISSN 2229-5178. PMC 5372441. PMID 28405561.
- ^ a b Vergani, Raffaella; Betti, Roberto; Martino, Patrizia; Crosti, Carlo (2002). "Giant Nevoid Hypertrichosis in an Iranian Girl". Pediatric Dermatology. 19 (1). Wiley: 64–66. doi:10.1046/j.1525-1470.2002.01970.x. ISSN 0736-8046. PMID 11860575.
- ^ a b c Chang, Sung Nam; Hong, Chang Eui; Kim, Dong-Kun; Park, Wook Hwa (1997). "A Case of Multiple Nevoid Hypertrichosis". The Journal of Dermatology. 24 (5). Wiley: 337–341. doi:10.1111/j.1346-8138.1997.tb02801.x. ISSN 0385-2407. PMID 9198325.
- ^ a b TE, Dudding; M, Rogers; LG, Roddick; J, Relic; MJ, Edwards (1998). "Nevoid hypertrichosis with multiple patches of hair that underwent almost complete spontaneous resolution". American Journal of Medical Genetics. 79 (3). Am J Med Genet: 195–196. doi:10.1002/(sici)1096-8628(19980923)79:3<195::aid-ajmg8>3.0.co;2-m. ISSN 0148-7299. PMID 9788560. Retrieved 2024-04-23.
- ^ Gupta, Lipy; Bharadwaj, Minakshi; Gautam, RamKishan (2011). "Nevoid hypertrichosis: Case report with review of the literature". International Journal of Trichology. 3 (2). Medknow: 115–117. doi:10.4103/0974-7753.90829. ISSN 0974-7753. PMC 3250008. PMID 22223975.
- ^ Koch, D.; Pratsou, P.; Szczecinska, W.; Lanigan, S.; Abdullah, A. (2013-10-31). "The diverse application of laser hair removal therapy: a tertiary laser unit's experience with less common indications and a literature overview". Lasers in Medical Science. 30 (1). Springer Science and Business Media LLC: 453–467. doi:10.1007/s10103-013-1464-5. ISSN 0268-8921. PMID 24173910.
Further reading
[edit]- Sotiriadis, Dimitrios; Patsatsi, Aikaterini; Lazaridou, Elizabeth; Sotiriou, Eleni; Devliotou-Panagiotidou, Despina (2009). "Multiple Nevoid Hypertrichosis as An Isolated Developmental Defect". Pediatric Dermatology. 26 (4). Wiley: 436–438. doi:10.1111/j.1525-1470.2009.00948.x. ISSN 0736-8046. PMID 19689520.
- Cox, N.H.; McCLURE, J.P.; Hardie, R.A. (1989). "Naevoid hypertrichosis-report of a patient with multiple lesions". Clinical and Experimental Dermatology. 14 (1): 62–64. doi:10.1111/j.1365-2230.1989.tb00887.x. ISSN 0307-6938. PMID 2805390.