Cutis laxa

{{Short description|Skin which is abnormally inelastic and hangs loosely}}

{{Redirect|Dermatochalasia|the medical condition affecting eyelids|Dermatochalasis}}

{{Infobox medical condition (new)

| name = Cutis laxa

| image = Ajcr-5-3.f1.jpg

| alt =

| caption = Cutis laxa in a neonate

| pronounce =

| field =

| synonyms = Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized elastolysis, Generalized elastorrhexis

| symptoms =

| complications =

| onset =

| duration =

| types =

| causes =

| risks =

| diagnosis =

| differential =

| prevention =

| treatment =

| medication =

| prognosis =

| frequency =

| deaths =

}}

Cutis laxa {{cite book | last1 = Rapini | first1 = Ronald P. | last2 = Bolognia | first2 = Jean L. | last3 = Jorizzo | first3 = Joseph L. | name-list-style = vanc |title=Dermatology: 2-Volume Set |publisher=Mosby |location=St. Louis |year=2007 |isbn=978-1-4160-2999-1 }} or pachydermatocele{{cite book | first1 = William D | last1 = James | first2 = Dirk M | last2 = Elston | first3 = Timothy G | last3 = Berger | first4 = George Clinton | last4 = Andrews | name-list-style = vanc | title = 'Andrews' Diseases of the Skin: Clinical Dermatology' | year = 1969 | edition = 10th | publisher = Saunders | page = 515 | isbn = 0-7216-2921-0 }} is a group of rare connective tissue disorders in which the skin becomes inelastic and hangs loosely in folds.{{cite book| vauthors = Millington P |title=Skin|date=2009|publisher=Cambridge University Press|isbn=978-0-521-10681-8|page=100}}

Signs and symptoms

It is characterised by skin that is loose, hanging, wrinkled, and lacking in elasticity. The loose skin can be either generalised or localised.{{cite journal | vauthors = Nygaard RH, Maynard S, Schjerling P, Kjaer M, Qvortrup K, Bohr VA, Rasmussen LJ, Jemec GB, Heidenheim M | display-authors = 6 | title = Acquired Localized Cutis Laxa due to Increased Elastin Turnover | journal = Case Reports in Dermatology | volume = 8 | issue = 1 | pages = 42–51 | date = 2016-02-13 | pmid = 27293393 | pmc = 4899661 | doi = 10.1159/000443696 }} Biopsies have shown reduction and degeneration of dermal elastic fibres in the affected areas of skin.{{cite journal | vauthors = García-Patos V, Pujol RM, Barnadas MA, Pérez M, Moreno A, Condomines J, Gelpi C, Rodríguez JL, De Moragas JM | display-authors = 6 | title = Generalized acquired cutis laxa associated with coeliac disease: evidence of immunoglobulin A deposits on the dermal elastic fibres | journal = The British Journal of Dermatology | volume = 135 | issue = 1 | pages = 130–4 | date = July 1996 | pmid = 8776377 | doi = 10.1046/j.1365-2133.1996.d01-950.x | s2cid = 38392112 }} The loose skin is often most noticeable on the face, resulting in a prematurely aged appearance. The affected areas of skin may be thickened and dark. In addition, the joints may be loose (hypermobile) because of lax ligaments and tendons. When cutis laxa is severe, it can also affect the internal organs. The lungs, heart (supravalvular pulmonary stenosis), intestines, or arteries may be affected with a variety of severe impairments. In some cases, hernias and outpouching of the bladder can be observed. Patients can also present with whites of the eyes that are blue.{{cn|date=September 2021}}

Causes

In many cases, cutis laxa is inherited. Autosomal dominant, autosomal recessive, and X-linked recessive forms have been described, but acquired forms also occur.{{cn|date=September 2021}}

Cutis laxa is associated with deficient or absent elastin fibers in the extracellular matrix.{{cite book | author = Plopper G | title = The extracellular matrix and cell adhesion, in Cells (eds Lewin B, Cassimeris L, Lingappa V, Plopper G) | location = Sudbury, MA | publisher = Jones and Bartlett | year = 2007 | isbn = 978-0-7637-3905-8 | url-access = registration | url = https://archive.org/details/cells0000unse }} This can be related to decreased elastin synthesis or structural defects in the extracellular matrix.{{cite journal | vauthors = Nygaard RH, Maynard S, Schjerling P, Kjaer M, Qvortrup K, Bohr VA, Rasmussen LJ, Jemec GB, Heidenheim M | display-authors = 6 | title = Acquired Localized Cutis Laxa due to Increased Elastin Turnover | journal = Case Reports in Dermatology | volume = 8 | issue = 1 | pages = 42–51 | date = 2016-02-13 | pmid = 27293393 | pmc = 4899661 | doi = 10.1159/000443696 }}

Cutis laxa may be caused by mutations in the genes: ELN,{{OMIM|123700|Cutis Laxa, Autosomal Dominant}} ATP6V0A2,{{OMIM|219200|Cutis Laxa, Autosomal Recessive, Type II}}

ATP7A,{{OMIM|304150|Cutis Laxa, X-Linked}} FBLN4,{{OMIM|219100|Cutis Laxa, Autosomal Recessive, Type I}} FBLN5,{{OMIM|604580|Fibulin 5; FBLN5}} and PYCR1.{{OMIM|179035|Pyrroline-5-Carboxylate Reductase 1; PYCR1 }} A related neurocutaneous syndrome may be caused by mutations in the gene ALDH18A1 (P5CS).{{OMIM|138250|Aldehyde Dehydrogenase 18 Family, Member A1; ALDH18A1 }} Cutis laxa may also be seen in association with inherited connective tissue disorders such as Ehlers–Danlos syndromes. Another syndrome associated with cutis laxa is Lenz-Majewski syndrome which is due to a mutation in the phosphatidylserine synthase 1 (PTDSS1) gene. {{cn|date=September 2021}}

In contrast, acquired cutis laxa often has a triggering event such as urticaria, drugs (such as penicillin) or neoplasms.{{cite journal | vauthors = Reddy GP, Mishra B, Upadhyaya DN | title = Acquired Localized Cutis Laxa: A Case Report and the Role of Plastic Surgery | journal = Indian Journal of Dermatology | volume = 64 | issue = 1 | pages = 55–58 | date = 2019 | pmid = 30745636 | pmc = 6340237 | doi = 10.4103/ijd.IJD_14_18 | doi-access = free }} Acquired cutis laxa may also be immunologically mediated, as it can involve dermal deposit of immunoglobulins and it can occur with autoimmune diseases. Acquired cutis laxa has been associated with granular immunoglobulin A deposits as well as abundant neutrophils. One hypothesis for the cause is excessive elastase release from neutrophils and macrophages. It has also been considered that mutations in elastin (ELN) and fibulin-5 (FBLN5) genes can increase susceptibility of elastic fibres to inflammatory degradation in acquired cutis laxa.

Acquired cutis laxa has also been seen in conjunction with a number of conditions including: rheumatoid arthritis,{{cite journal | vauthors = Rongioletti F, Cutolo M, Bondavalli P, Rebora A | title = Acral localized acquired cutis laxa associated with rheumatoid arthritis | journal = Journal of the American Academy of Dermatology | volume = 46 | issue = 1 | pages = 128–30 | date = January 2002 | pmid = 11756959 | doi = 10.1067/mjd.2002.117394 }} systemic lupus erythematosus,{{cite journal | vauthors = Randle HW, Muller S | title = Generalized elastolysis associated with systemic lupus erythematosus | language = English | journal = Journal of the American Academy of Dermatology | volume = 8 | issue = 6 | pages = 869–73 | date = June 1983 | pmid = 6345611 | doi = 10.1016/S0190-9622(83)80019-X }} celiac disease, and monoclonal gammopathies.{{cite journal | vauthors = Maruani A, Arbeille B, Machet MC, Barbet C, Laure B, Martin L, Machet L | title = Ultrastructural demonstration of a relationship between acquired cutis laxa and monoclonal gammopathy | journal = Acta Dermato-Venereologica | volume = 90 | issue = 4 | pages = 406–8 | date = July 2010 | pmid = 20574607 | doi = 10.2340/00015555-0887 | doi-access = free }} It can also occur as a postinflammatory response after urticaria.{{cite journal | vauthors = Nygaard RH, Maynard S, Schjerling P, Kjaer M, Qvortrup K, Bohr VA, Rasmussen LJ, Jemec GB, Heidenheim M | display-authors = 6 | title = Acquired Localized Cutis Laxa due to Increased Elastin Turnover | journal = Case Reports in Dermatology | volume = 8 | issue = 1 | pages = 42–51 | date = 2016-02-13 | pmid = 27293393 | pmc = 4899661 | doi = 10.1159/000443696 }} Urticarial skin fibroblasts have shown a 2- to 3- fold increase in elastase activity in a patient with acquired cutis laxa.{{cite journal | vauthors = Bouloc A, Godeau G, Zeller J, Wechsler J, Revuz J, Cosnes A | title = Increased fibroblast elastase activity in acquired cutis laxa | language = english | journal = Dermatology | volume = 198 | issue = 4 | pages = 346–50 | date = 1999 | pmid = 10449932 | doi = 10.1159/000018146 | s2cid = 23679878 }}

Diagnosis

Treatment

As of 2024, there is no treatment for cutis laxa. Procedures aimed at mitigating symptoms and identifying subsequent conditions are often advised. No pharmacological agent has been able to stop the progression of the disease. However, cosmetic surgeries are potentially an option as cutis laxa does not generally involve vascular fragility.

References

External links

{{Medical resources

| DiseasesDB = 29439

| ICD10 = {{ICD10|L|57|4|l|55}}, {{ICD10|Q|82|8|q|80}} (ILDS Q82.816)

| ICD9 = {{ICD9|701.8}}, {{ICD9|756.83}}

| ICDO =

| OMIM = 123700

| OMIM_mult = {{OMIM|219100||none}} {{OMIM|219200||none}} {{OMIM|304150||none}}

| MedlinePlus =

| eMedicineSubj = derm

| eMedicineTopic = 03

| MeshID = D003483

| GeneReviewsNBK = NBK5201

| GeneReviewsName = FBLN5-Related Cutis Laxa

| Orphanet = 209

}}

[http://emedicine.medscape.com/article/1074167-overview Medscape entry on Cutis Laxa]

Category:Abnormalities of dermal fibrous and elastic tissue

Category:Rare diseases