256 results match your criteria Steatocystoma Multiplex


A simple modified surgical technique combined with tissue adhesive for steatocystoma multiplex.

J Cosmet Dermatol 2020 May 10. Epub 2020 May 10.

Department of Dermatologic Surgery, Shanghai Skin Diseases Hospital, Shanghai, China.

Background: Steatocystoma multiplex (SM) is a disorder of the pilosebaceous unit characterized by multiple sebum-containing dermal cysts. Psychological distress of patients is always derived from these undesirable lesions. Although various treatments have been attempted to improve cosmetic outcomes, no optimal treatment strategy has been established to date. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/jocd.13438DOI Listing
May 2020
1.000 Impact Factor

Ultrasound Morphologic Features of Steatocystoma Multiplex With Clinical Correlation.

J Ultrasound Med 2020 May 1. Epub 2020 May 1.

Department of Dermatology, Universidad de Chile, Santiago, Chile.

The ultrasound features of 87 steatocytoma multiplex (SCM) lesions detected in 9 patients are reported. Steatocytoma multiplex is a hamartomatous condition derived from the pilosebaceous duct junction that generates multiple cutaneous cystic lesions. It appeared as clusters of well-defined hypoechoic nodules with mild posterior enhancement in 100% of cases, with both dermal and subcutaneous locations in 67%. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/jum.15320DOI Listing

Steatocystoma multiplex: A case report of a rare entity.

Imaging Sci Dent 2019 Dec 24;49(4):317-321. Epub 2019 Dec 24.

Department of Oral and Maxillofacial Radiology and Dental Research Institute, School of Dentistry, Seoul National University, Seoul, Korea.

Steatocystoma multiplex is an uncommon benign skin disease, which typically manifests as numerous intradermal cysts that can be scattered anywhere on the body. Although usually asymptomatic, it can be significantly disfiguring. One type of steatocystoma multiplex is known to be associated with the autosomal dominant inheritance of a mutation in the gene coding for keratin 17 (). Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5624/isd.2019.49.4.317DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941837PMC
December 2019

Steatocystoma multiplex suppurativa associated with hidradenitis suppurativa successfully treated with adalimumab.

J Eur Acad Dermatol Venereol 2019 Oct;33 Suppl 6:42-44

Section of Dermatology, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.

Steatocystoma multiplex (SM) is a rare autosomal dominant disease characterized by multiple asymptomatic intradermal true sebaceous cysts of variable size. These lesions may occasionally rupture, become inflamed, painful and heal with scarring [SM suppurativa (SMS)], thus sharing overlapping features with hidradenitis suppurativa (HS). The question of whether SMS simply mimics HS or if the two diseases may be associated remains open. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/jdv.15848DOI Listing
October 2019
14 Reads

Dermatoscopy for the rapid diagnosis of Talaromyces marneffei infection: a case report.

BMC Infect Dis 2019 Aug 9;19(1):707. Epub 2019 Aug 9.

Department of Dermatology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.

Background: Talaromyces marneffei is a thermally dimorphic fungus endemic in south-east Asia. It predominantly occurs in both immunocompromised and immunosuppressed patients and can be fatal if diagnosis and treatment are delayed. The clinical manifestations of T. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12879-019-4351-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689180PMC
August 2019
4 Reads

Coexistence of steatocystoma multiplex and hidradenitis suppurativa: Assessment of this unique association by means of ultrasonography and Color Doppler.

Skin Res Technol 2019 Nov 28;25(6):877-880. Epub 2019 Jul 28.

UOC Dermatologia, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

Background: Steatocystoma multiplex (SM) is an uncommon skin disease manifesting as multiple sebum-containing cysts arising in pilosebaceous unit-rich body areas. Hidradenitis suppurativa (HS) is a debilitating chronic inflammatory disease affecting the apocrine gland-bearing skin and presenting with both pseudocystic and inflammatory nodules, abscesses and fistulas. Considering that genetics has been reported to play a role in both entities, the albeit rare association between them suggests a shared genetic background. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/srt.12751DOI Listing
November 2019
1 Read

Mutation analysis of the KRT17 gene in steatocystoma multiplex and a brief literature review.

Clin Exp Dermatol 2020 Jan 17;45(1):132-134. Epub 2019 Sep 17.

Shandong Provincial Hospital for Skin Diseases, Shandong University, 27397 Jingshi Road, Jinan, Shandong, 250022, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ced.14030DOI Listing
January 2020
10 Reads

Steatocystoma Multiplex Suppurativa: A Case with Unusual Giant Cysts over the Scalp and Neck.

Case Rep Dermatol 2019 Jan-Apr;11(1):71-76. Epub 2019 Mar 19.

Department of Dermatology, King Saud University Medical City, Riyadh, Saudi Arabia.

Steatocystoma multiplex (SM) is a rare hamartomatous malformation of the pilosebaceous duct junction. Most cases of SM are sporadic, although less common autosomal dominant inherited forms have been reported. Steatocystoma multiplex suppurativa (SMS) is a much rarer inflammatory variant of SM, associated with severe inflammatory lesions resembling those of hidradenitis suppurativa. Read More

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/498882
Publisher Site
http://dx.doi.org/10.1159/000498882DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465725PMC
March 2019
52 Reads

1927-nm fiber-optic diode laser: A novel therapeutic option for facial steatocystoma multiplex.

J Cosmet Dermatol 2018 Dec 30. Epub 2018 Dec 30.

Department of Dermatology, College of Medicine, University of Hanyang, Seoul, Korea.

Steatocystoma multiplex (SM) is a cutaneous disorder that presents with multiple yellowish intradermal cysts originating from the pilosebaceous ducts. Although various treatments have been attempted to improve cosmetic outcomes, no optimal treatment strategy has been established to date. A 41-year-old man presented with a 10-year history of multiple skin-colored papulonodules over his entire body. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/jocd.12849DOI Listing
December 2018
32 Reads

Numerous asymptomatic dermal cysts: Diagnosis and treatment of steatocystoma multiplex.

Can Fam Physician 2018 12;64(12):892-899

Lecturer and staff dermatologist in the Division of Dermatology at the University of Toronto.

Objective: To provide family physicians with the information needed to recognize, diagnose, and discuss available treatment options for steatocystoma multiplex (SM).

Sources Of Information: A comprehensive PubMed search using as either a text word or a MeSH term was conducted, and articles reporting on treatment outcomes were included.

Main Message: Steatocystoma multiplex is a benign disorder often characterized by numerous asymptomatic dermal cysts on the trunk, arms, axillae, face, thighs, and scalp. Read More

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371868PMC
December 2018
55 Reads
1.403 Impact Factor

Treatment of steatocystoma multiplex on axillae using keyhole approach technique.

J Cosmet Laser Ther 2019 16;21(4). Epub 2018 Oct 16.

Department of Dermatology, Ho Wen Tsao Skin Clinic , New Taipei City , Taiwan, ROC.

View Article

Download full-text PDF

Source
https://www.tandfonline.com/doi/full/10.1080/14764172.2018.1
Publisher Site
http://dx.doi.org/10.1080/14764172.2018.1525746DOI Listing
March 2020
27 Reads

Keratin 17 in disease pathogenesis: from cancer to dermatoses.

J Pathol 2019 02 7;247(2):158-165. Epub 2018 Dec 7.

Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an, PR, China.

Keratin 17 (K17) is a type I intermediate filament mainly expressed in the basal cells of epithelia. As a multifaceted cytoskeletal protein, K17 regulates a myriad of biological processes, including cell proliferation and growth, skin inflammation and hair follicle cycling. Aberrant overexpression of K17 is found in various diseases ranging from psoriasis to malignancies such as breast, cervical, oral squamous and gastric carcinomas. Read More

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/path.5178
Publisher Site
http://dx.doi.org/10.1002/path.5178DOI Listing
February 2019
33 Reads

Steatocystoma Simplex on the Scalp: A Case Report.

Mymensingh Med J 2018 Jul;27(3):669-671

Dr Fahmida Akter Rima, Lecturer, Department of Pathology, Dhaka Medical College, Dhaka, Bangladesh.

Steatocystoma is a benign adnexal tumor arising from the pilosebaceous duct junction. It can be classified into two groups (steatocystoma simplex and steatocystoma multiplex). Steatocystoma simplex, which presents as a solitary, non-herited very rare lesion in adult. Read More

View Article

Download full-text PDF

Source
July 2018
87 Reads

An Unusual Case of Facial Steatocystoma Multiplex: A Clinicopathologic and Dermoscopic Report.

Dermatopathology (Basel) 2018 Apr-Jun;5(2):58-63. Epub 2018 May 22.

Department of Dermatology, Lokmanya Tilak Municipal Medical College (LTMMC) and Sion General Hospital, Mumbai, India.

Background: Steatocystoma multiplex is a benign skin disorder originating from the sebaceous and nevoid ducts. Commonly classified under hamartomas, they are distributed over the trunk, neck, axillae, and groin.

Methods: A 28-year-old male patient complained of multiple, asymptomatic skin-colored nodules over the face of 10-year duration. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000488584DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031952PMC
May 2018
171 Reads

A novel APC mutation identified in a large Chinese family with familial adenomatous polyposis and a brief literature review.

Mol Med Rep 2018 Aug 5;18(2):1423-1432. Epub 2018 Jun 5.

Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, Sichuan 610072, P.R. China.

Familial adenomatous polyposis (FAP), an autosomal dominant disease, is a colon cancer predisposition syndrome that manifests as a large number of adenomatous polyps. Mutations in the Adenomatous polyposis coli (APC) gene are responsible for the majority of cases of FAP. The purpose of the present study was to report the clinical features of a Chinese family with FAP and screen for novel mutations using the targeted next‑generation sequencing technology. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3892/mmr.2018.9130DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072187PMC
August 2018
33 Reads

Eruptive Vellus Hair Cyst: An Uncommon and Underdiagnosed Entity.

Int J Trichology 2018 Jan-Feb;10(1):31-33

Department of Dermatology, Hindu Rao Hospital and NDMC Medical College, NewDelhi, India.

Eruptive vellus hair cyst (EVHC) is a rare follicular developmental abnormality of the vellus hair follicles. They are usually seen in children, adolescents, or young adults and manifest as reddish-brown smooth papules most commonly involving the chest, limbs, and abdomen. An 18-year-old male presented with asymptomatic papules on the trunk and flexor aspect of both forearms for the past 2 years. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/ijt.ijt_61_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803851PMC
February 2018
43 Reads

Cutaneous Cysts with Nail Dystrophy in a Young Female: A Classical Association.

Indian J Dermatol 2017 Nov-Dec;62(6):661-664

Department of Dermatology, Venereology and Leprosy, School of Tropical Medicine, Kolkata, West Bengal, India.

Pachyonychia Congenita (PC) refers to a group of autosomal dominant disorders with variable clinical presentations. While nail dystrophy and plantar keratoderma are the most consistent features in all the variants, a myriad of other manifestations has been observed. This report highlights a case of young female presenting with multiple asymptomatic cutaneous cysts associated with plantar kearatoderma and nail dystrophy. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/ijd.IJD_473_16DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724318PMC
December 2017
22 Reads

A recurrent mutation in the KRT17 gene responsible for severe steatocystoma multiplex in a large Chinese family.

Clin Exp Dermatol 2018 Mar 8;43(2):205-208. Epub 2017 Dec 8.

Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ced.13311DOI Listing
March 2018
17 Reads

Co-occurrence of steatocystoma multiplex, eruptive vellus hair cysts, and trichofolliculomas.

Cutis 2017 Jul;100(1):E23-E26

Department of Dermatology and the Department of Laboratory Medicine, Mayo Clinic, Rochester, Minnesota, USA.

An association between steatocystoma multiplex (SCM) and eruptive vellus hair cysts (EVHCs) has been recognized. Steatocystoma multiplex and EVHC have similar clinical features but distinctive histologic features. Rare cases of co-occurrence of these conditions have been known to occur on the trunk and the forehead. Read More

View Article

Download full-text PDF

Source
July 2017
22 Reads

Case Series: A Kindred With Eruptive Vellus Hair Cysts and Systemic Features.

J Cutan Med Surg 2017 Nov/Dec;21(6):564-567. Epub 2017 Jun 28.

1 Department of Dermatology and Skin Science, University of British Columbia, Vancouver, British Columbia, Canada.

Eruptive vellus hair cysts (EVHCs) often occur on the trunk and limbs. Facial involvement is uncommon. Autosomal dominant inheritance has been described, but associated extracutaneous anomalies have not. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1203475417719044DOI Listing
July 2018
44 Reads

A Tale of Two Cysts: Steatocystoma Multiplex and Eruptive Vellus Hair Cysts-Two Case Reports and a Review of the Literature.

Case Rep Dermatol Med 2017 5;2017:3861972. Epub 2017 Apr 5.

College of Medicine, University of Illinois-Chicago, Urbana Campus, 506 South Mathews Ave., 190 Medical Sciences Building, MC-714, Urbana, IL 61801, USA.

. Steatocystoma multiplex (SM) and eruptive vellus hair cysts (EVHC) are uncommon benign tumors of the pilosebaceous unit. Both SM and EVHC are characterized by smooth, asymptomatic papules or nodules, most commonly presenting on the chest, limbs, and abdomen. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2017/3861972DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396452PMC
April 2017
18 Reads

Steatocystoma multiplex suppurativa: case report of a rare condition.

An Bras Dermatol 2016 Sep-Oct;91(5 suppl 1):51-53

Universidade do Estado do Rio de Janeiro (UERJ) - Rio de Janeiro (RJ), Brazil.

Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1590/abd1806-4841.20164539DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324992PMC
July 2017
23 Reads

Difficult diagnosis and challenging treatment – a report on leprosy.

Lepr Rev 2016 Dec;87(4):543-7

Histoid leprosy is an unusual variant of lepromatous leprosy posing difficulties for diagnosis as well as treatment even to the experts. We report a case of a 73 year old male from the hilly region of Nepal, who presented with multiple asymptomatic scrotal nodules for 3 months. Though clinical diagnoses were pilomatricoma and steatocystoma multiplex; histopathological examination was consistent with that of histoid leprosy. Read More

View Article

Download full-text PDF

Source
December 2016
13 Reads

Pachyonychia congenita with late onset (PC tarda).

Indian Dermatol Online J 2016 Jul-Aug;7(4):278-80

Department of Dermatology, Maharajah's Institute of Medical Sciences, Nellimarla, Andhra Pradesh, India.

Pachyonychia congenita is a rare type of ectodermal dysplasia further classified into 4 types. Cutaneous manifestations seen in most of the cases of Pachyonychia congenita include palmoplantar keratoderma, follicular hyperkeratosis, wedge shaped nails, oral leukokeratosis and woolly hair. A 25-year-old male presented to us with thickened nails and scanty scalp hair. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/2229-5178.185463DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976406PMC
August 2016
35 Reads

Fractionated ablative carbon dioxide laser treatment of steatocystoma multiplex.

J Cosmet Laser Ther 2016 Nov 19;18(7):364-366. Epub 2016 Jul 19.

b Department of Dermatology , University of California Irvine , Irvine , CA , USA.

Steatocystoma multiplex is a well-recognized condition in which subjects develop dermal cysts generally inherited in an autosomal dominant fashion, though these can occur sporadically. This case report describes the successful treatment of a 51-year-old woman with steatocystomata limited to the face, who after two treatments with a fractionated ablative carbon dioxide laser remained free of cysts for three years. We conclude that this treatment should be considered as an efficient and effective treatment option for patients with steatocystoma multiplex. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/14764172.2016.1188212DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739516PMC
November 2016
95 Reads

Steatocystoma simplex in penile foreskin: a case report.

J Med Case Rep 2016 Mar 8;10:49. Epub 2016 Mar 8.

Biodiversity Research Center, Federal University of Roraima (CBio/UFRR), Boa Vista - RR, Brazil.

Background: Steatocystoma simplex is an uncommon skin lesion with a histological pattern that is identical to that of steatocystoma multiplex. We are reporting this case of steatocystoma simplex for its uncommon location in the penile foreskin, and its occurrence in a Wapishana man.

Case Presentation: A 56-year-old man of Wapishana ethnicity presented with complaints of referred penile discomfort and pain during sexual intercourse for 5 years. Read More

View Article

Download full-text PDF

Source
http://jmedicalcasereports.biomedcentral.com/articles/10.118
Publisher Site
http://dx.doi.org/10.1186/s13256-016-0845-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782336PMC
March 2016
82 Reads

Clinical Misdiagnosis of Steatocystoma Simplex of Eyebrow in a Pediatric Patient.

Chin Med J (Engl) 2016 Feb;129(3):377-8

Institute of Plastic and Craniofacial Surgery, SOBRAPAR Hospital, Campinas, São Paulo, Brazil.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/0366-6999.174493DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799590PMC
February 2016
13 Reads

Steatocystoma multiplex is associated with the R94C mutation in the KRTl7 gene.

Mol Med Rep 2015 Oct 8;12(4):5072-6. Epub 2015 Jul 8.

Department of Dermatology, Hainan Provincial Hospital of Skin Disease, Haikou, Hainan 570206, P.R. China.

Steatocystoma multiplex (SM) is an uncommon disorder, characterized by numerous skin‑colored subcutaneous cysts. A number of SM pedigrees have been identified with mutations in the keratin 17 (KRT17) gene. The present study examined a four‑generation Chinese pedigree with an autosomal dominant mode of inheritance and examined its genetic basis. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3892/mmr.2015.4063DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581757PMC
October 2015
48 Reads

Timed exposure 10,600 nm CO2 laser drilling in various benign dermal tumours.

Eur J Dermatol 2015 Jul-Aug;25(4):358-9

Netherlands Institute for Pigment Disorders (SNIP),, Department of Dermatology, Academic Medical Center, Meibergdreef 9, 1105AZ, Amsterdam, the Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/ejd.2015.2583DOI Listing
June 2016
25 Reads

Association of copeptin and cortisol in newly diagnosed multiple sclerosis patients.

J Neuroimmunol 2015 May 11;282:21-4. Epub 2015 Mar 11.

Department of Neuroendocrinology, Centre of Postgraduate Medical Education, Marymoncka 99/103, 01-813 Warsaw, Poland. Electronic address:

Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system. Obesity may increase the risk of developing MS. The aim of this study was to evaluate copeptin and cortisol plasma levels in newly diagnosed untreated MS patients and to determine whether copeptin and cortisol are related to the patients' clinical statuses. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jneuroim.2015.03.011DOI Listing
May 2015
18 Reads

Steatocystoma multiplex with hair shaft abnormalities.

J Dermatol 2015 May 21;42(5):521-3. Epub 2015 Mar 21.

Department of Dermatology, Venereology and Pediatric Dermatology, Medical University of Lublin, Lublin, Poland.

Steatocystoma multiplex (SM) is an unusual benign disorder of the pilosebaceous duct characterized by multiple cysts with little or no nail and hair involvement. We report a 30-year-old woman with multiple cystic nodules located on the neck, axillae and forearms as well as patchy scalp alopecia. Histopathological examination of the lesions was diagnostic of SM. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/1346-8138.12837DOI Listing
May 2015
15 Reads
2.354 Impact Factor

Steatocystoma multiplex: those little tumours.

Skinmed 2014 Sep-Oct;12(5):267-9

View Article

Download full-text PDF

Source
February 2015
66 Reads

Polycystic kidney disease with steatocystoma multiplex: evidences for a disruptive effect of mutated polycystin-1 on keratin 17 polymerisation.

Acta Derm Venereol 2015 Mar;95(3):353-4

Department of Dermatology, Faculty of Medicine, Kagawa University, 1750-1 Ikenobe, Kita-gun Miki-cho, 761-0793 Kagawa, Japan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2340/00015555-1934DOI Listing
March 2015
19 Reads

Facial steatocystoma multiplex combined with eruptive vellus hair cysts: a hybrid?

J Eur Acad Dermatol Venereol 2015 Oct 30;29(10):2051-3. Epub 2014 Jul 30.

Department of Dermatology und Venereology, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/jdv.12588
Publisher Site
http://dx.doi.org/10.1111/jdv.12588DOI Listing
October 2015
25 Reads

On Steatocystoma, Sebaceous Duct Cyst, Isthmic-Anagenic Cyst, and CK19.

Am J Dermatopathol 2015 Sep;37(9):733-4

Department of Cellular Pathology, Hospital El Bierzo, Ponferrada, Spain.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000000186DOI Listing
September 2015
10 Reads

Cutaneous keratocyst and steatocystoma unified as sebaceous duct cyst, a hamartoma resembling the sebaceous duct.

Authors:
Mani Makhija

Am J Dermatopathol 2015 Nov;37(11):871-3

Department of Histopathology, National Reference Laboratory, Dr Lal Pathlabs, Delhi, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000000176DOI Listing
November 2015
11 Reads

Carbon dioxide laser perforation and extirpation of steatocystoma multiplex.

Dermatol Surg 2014 Jun;40(6):658-62

*Both the authors are affiliated with the Manchester Laser Unit, Dermatology Centre, Salford Royal NHS Foundation Trust, Manchester, United Kingdom.

Background: Steatocystoma multiplex (SM) is a rare condition that presents as multiple dermal cysts, the appearance of which can have a significant impact on the patients' quality of life. Treatment options for SM are limited to surgical excision.

Objective: To present our experience of treating 8 SM cases using a novel approach that uses the carbon dioxide (CO2) laser and to explore patients' views about the treatment. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/dsu.0000000000000013DOI Listing
June 2014
22 Reads

Familial pachyonychia congenita with steatocystoma multiplex and multiple abscesses of the scalp due to the p.Asn92Ser mutation in keratin 17.

Br J Dermatol 2014 Dec 2;171(6):1565-7. Epub 2014 Nov 2.

Department of Dermatology, Montauban Hospital, Montauban, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjd.13123DOI Listing
December 2014
26 Reads

Recurring axillary, abdominal and genitofemoral nodules and abscesses. Hereditary steatocystoma multiplex.

Acta Derm Venereol 2015 Jan;95(1):121-3

Department of Dermatology, Roskilde Hospital, Health Sciences Faculty, University of Copenhagen, Køgevej 7-13, DK-4000 Roskilde, Denmark.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2340/00015555-1890DOI Listing
January 2015
26 Reads

Steatocystoma multiplex associated with bilateral preauricular sinuses.

J Cutan Pathol 2014 Aug 19;41(8):677-9. Epub 2014 Mar 19.

Department of Cellular Pathology, Hospital El Bierzo, Ponferrada, Spain.

Steatocystoma multiplex is characterized by the development of numerous steatocystomas. The condition has occasionally been related to congenital bilateral preauricular sinuses. Herein, we present the third case of such an association, a 34-year-old male who was born with bilateral preauricular sinuses that were surgically repaired. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cup.12315DOI Listing
August 2014
52 Reads

Steatocystoma multiplex as initial impression of non-small cell lung cancer with complete response to gefitinib.

Chin J Cancer Res 2014 Feb;26(1):E5-9

1 Department of Internal Medicine, 2 Department of Dermatology, 3 Department of Pathology, Chung Shan Medical University Hospital and School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan, China.

Cutaneous metastases are rare and seldom present at the time of first diagnosis of cancer. Data from various studies show that 1-12% of lung cancer patients experience tumor spread to the skin. The scalp, chest, and abdomen are favored sites of skin metastases from lung cancers, but metastases to multiple skin sites in a single patient are rarely reported. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3978/j.issn.1000-9604.2014.01.02DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937749PMC
February 2014
16 Reads

Late onset localized steatocystoma multiplex of the vulva.

Indian J Dermatol Venereol Leprol 2014 Jan-Feb;80(1):89-90

Department of Dermatology, Chonbuk National University Medical School; Research Institute of Clinical Medicine of Chonbuk National University Biomedical Research Institute of Chonbuk National University Hospital, Jeonju, South Korea.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/0378-6323.125495DOI Listing
April 2016
14 Reads

A novel missense mutation of keratin 17 gene in a chinese family with steatocystoma multiplex.

Ann Dermatol 2013 Nov 30;25(4):508-10. Epub 2013 Nov 30.

Institute of Dermatology, Anhui Medical University, Hefei, Anhui, China. ; The MOE Key Laboratory of Dermatology, Hefei, Anhui, China. ; Department of Dermatology and Venereology, the First Affiliated Hospital, Anhui Medical University, Hefei, Anhui, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.5021/ad.2013.25.4.508DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870228PMC
November 2013
20 Reads

Steatocystoma.

Dermatol Online J 2013 Dec 16;19(12):20721. Epub 2013 Dec 16.

New York University School of Medicine.

Steatocystoma multiplex is a rare condition that is characterized by cutaneous cysts and may be inherited in an autosomal dominant manner or may occur sporadically. The pathogenesis is hypothesized to involve mutations in the keratin 17 gene. There are no internal manifestations. Read More

View Article

Download full-text PDF

Source
December 2013
34 Reads

Multiple cystic disease: K17 dysfunction?

Skinmed 2013 Sep-Oct;11(5):301-3

Dermatology Department, Hospital Nacional Profesor Alejandro Posadas, Buenos Aires, Argentina.

Our patient is a 29-year-old woman without any previous disease who presented with different kinds of lesions on her face, neck, and chest. She first noticed the lesions 10 years ago and, since that time, they have become more numerous. She has no affected relatives. Read More

View Article

Download full-text PDF

Source
January 2014
30 Reads

Increased FDG uptake in scrotal steatocystoma multiplex with calcification.

Clin Nucl Med 2014 Sep;39(9):822-4

From the Departments of *Nuclear Medicine, †Pathology, and ‡Respiratory Medicine, Changhai Hospital, Second Military Medical University, Shanghai, China.

Steatocystoma multiplex is a rare, benign, sporadic or familial disorder. Steatocystoma multiplex with extensive calcification is extremely rare. A 57-year-old man presented fever and cough with expectoration for 3 weeks. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/RLU.0000000000000300DOI Listing
September 2014
16 Reads

A rare case of facial steatocystoma multiplex.

Acta Dermatovenerol Croat 2013 ;21(3):205-6

Derya Uçmak, MD, Department of Dermatology, Dicle University Faculty of Medicine, Diyarbakir, Turkey;

View Article

Download full-text PDF

Source
August 2014
19 Reads

Nodular-cystic lesions on a congenital alopecic plaque.

Actas Dermosifiliogr 2014 Jan-Feb;105(1):85-6. Epub 2013 Oct 16.

Servicio de Dermatología, Hospital Gregorio Marañón, Madrid, España.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ad.2013.08.007DOI Listing
April 2015
10 Reads

Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis.

Authors:
Noah Scheinfeld

Dermatol Online J 2013 Jun 15;19(6):18558. Epub 2013 Jun 15.

Weill Cornell Medical College, New York, NY, USA.

Hidradenitis suppurativa (HS), a pathologic follicular disease, impacts patients' lives profoundly and usually occurs in isolation. The diseases with the strongest association are obesity, depression, and pain. HS is associated with many diseases including acne conglobata (AC), dissecting cellulitis, pilonidal cysts, and obesity. Read More

View Article

Download full-text PDF

Source
June 2013
34 Reads