910 results match your criteria Syringoma


Acral Eruptive Syringoma: An Unusual Presentation with Misdiagnosis.

Case Rep Dermatol Med 2020 11;2020:5416285. Epub 2020 Jan 11.

Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Eruptive syringoma is a rare variant of syringoma presenting with skin-colored or slightly pigmented papules mostly before or during puberty. In this report, we presented a rare case of eruptive syringoma in a 30-year-old woman. She exhibited multiple skin lesions in dorsal areas of her both hands, developed from the age of 15. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2020/5416285DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201436PMC
January 2020

Complete and Long-Term Clearance in Eruptive Syringoma With Fractional Nonablative Laser in Asian Skin.

Dermatol Surg 2020 Apr 28. Epub 2020 Apr 28.

Delhi Dermatology Group, New Delhi, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DSS.0000000000002424DOI Listing

and Fusion Genes in Chondroid Syringoma.

Cancer Genomics Proteomics 2020 May-Jun;17(3):237-248

Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

Background/aim: Chondroid syringoma is a rare benign tumor emanating from sweat glands. Although rearrangements of the pleomorphic adenoma gene 1 (PLAG1) have been reported in such tumors, information on PLAG1 fusion genes is very limited.

Materials And Methods: Cytogenetic, fluorescence in situ hybridization, RNA sequencing, array comparative genomic hybridization, reverse transcription polymerase chain reaction, and Sanger sequencing analyses were performed on two chondroid syringoma cases. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.21873/cgp.20184DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7259886PMC
January 2020

Visual Dermatology: Eruptive Vulvar Syringoma.

J Cutan Med Surg 2020 Mar/Apr;24(2):189

14655 Department of Dermatology, Faculty of Medicine, Universidad de Chile, Santiago, Chile.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1203475419888868DOI Listing

Chondroid syringoma of the axilla masquerading as a metastatic lymph node.

Breast J 2020 Feb 7. Epub 2020 Feb 7.

Department of Pathology, Chonnam National University Medical School, Chonnam National University Hwasun Hospital, Gwangju, Korea.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/tbj.13773DOI Listing
February 2020

Treatment of a case wıth gıant eyelıd syrıngomas.

Niger J Clin Pract 2020 Feb;23(2):273-274

Department of Pathology, Ufuk University, Ankara, Turkey.

He had a history of multiple asymptomatic flesh-colored papules, which had slowly increased in number and coalesced into plaques, on both upper and lower eyelids. Some of the plaques were giant and mostly coalescent in nature. We excised surgically the giant plaques which were approximately 1. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/njcp.njcp_115_19DOI Listing
February 2020

Syringoid Eccrine Carcinoma in the Abdominal Wall: A Rare Case Report and Literature Review.

Am J Case Rep 2019 Dec 19;20:1896-1901. Epub 2019 Dec 19.

Department of Pathology, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil.

BACKGROUND Syringoid eccrine carcinoma (SEC) is an extremely rare malignant adnexal neoplasm derived from eccrine sweat glands, of unknown pathogenesis. We report a case of this rare entity presenting in the abdomen, which is the only one reported in this area and the only case of SEC in a patient with so many comorbidities. CASE REPORT A 58-year-old black male from Brazil reported a nodular lesion in the abdomen with a progressive increase in size and pain and local burning sensation. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.12659/AJCR.919444DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930704PMC
December 2019

Malignant Chondroid Syringoma With Nose and Paranasal Sinus Extension: A Case Report.

Allergy Rhinol (Providence) 2019 Jan-Dec;10:2152656719893367. Epub 2019 Dec 3.

Department of ENT, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India.

Chondroid syringoma is a rare, skin appendageal tumor. It is also known as mixed tumor of skin, as it histologically resembles mixed tumor of salivary gland (pleomorphic adenoma). It is most commonly a benign tumor, but a few malignant counterparts have been described in history. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/2152656719893367DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893930PMC
December 2019

A Rare Forehead Mass: The Chondroid Syringoma.

Cureus 2019 Sep 25;11(9):e5763. Epub 2019 Sep 25.

Plastic Surgery, Columbia University College of Physicians and Surgeons at Harlem Hospital Center, New York, USA.

The chondroid syringoma is an extremely rare skin tumor most commonly found in the area of the head and neck region. Its rarity, potential for malignancy, and frequent misdiagnosis for other more common tumors can impart unique challenges in diagnosis and management. Diagnosis is usually revealed by excision followed by histologic examination. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.7759/cureus.5763DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6825454PMC
September 2019

Malignant Chondroid Syringoma: A Report of Two Cases with a Sarcomatous Mesenchymal Component.

Dermatopathology (Basel) 2019 Apr-Jun;6(2):77-84. Epub 2019 Jun 26.

Division of Anatomical Pathology, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Malignant chondroid syringoma (MCS; malignant mixed tumour) is a rare neoplasm typically arising on the extremities and trunk. We are report 2 unique cases of MCS, one occurring on the scalp of a 78-year-old man and the other on the trunk of a 72-year-old woman. Both tumours harboured malignant epithelial and malignant mesenchymal components. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000495610DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827459PMC

Tubular apocrine adenoma of the eyelid - A case report and literature review.

Saudi J Ophthalmol 2019 Jul-Sep;33(3):304-307. Epub 2019 Jul 26.

Department of Pathology, Wills Eye Hospital, Thomas Jefferson University, Philadelphia, PA, USA.

Tubular apocrine adenoma is a rare benign adnexal neoplasm most commonly identified in the scalp, composed of a dermal proliferation of apocrine tubules in a background of hyalinized stroma. Tubular apocrine adenoma can be a component of various sweat gland tumors and can also morphologically overlap with other sweat gland neoplasms. Isolated tubular apocrine adenoma arising in the glands of Moll is exceedingly rare, with only 4 previously reported cases. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.sjopt.2019.07.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6819710PMC

Post Treatment Application of Jaungo after a Combined Therapy of Carbon Dioxide Laser and Trichloroacetic Acid in a Case of Vulvar Syringoma.

J Pharmacopuncture 2019 Sep 30;22(3):200-203. Epub 2019 Sep 30.

Division of Pharmacology, College of Korean Medicine, Semyung University, Jecheon, South Korea.

Syringoma is a benign eccrine sweat gland tumor that predominantly appears in females during puberty with multiple smooth papules measuring 1-2 mm in diameter. Common locations are on lower eyelids and cheeks. Vulvar syringoma is quite a rare, occurring condition with only a few cases reported. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3831/KPI.2019.22.027DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820478PMC
September 2019
1 Read

Intralesional Electrocoagulation With Insulated Microneedle for the Treatment of Periorbital Syringomas: A Retrospective Analysis.

Aesthet Surg J 2019 Oct 21. Epub 2019 Oct 21.

Department of Dermatology, Chung-Ang University Hospital, Seoul, Korea.

Background: Conventional treatment options for periorbital syringomas are often unsatisfactory because of inevitable surface damages from the procedure and frequent recurrence rate of the tumors.

Objective: To ascertain the efficacy and safety of intralesional electrosurgery using a monopolar radiofrequency device with a single insulated microneedle for the treatment of periorbital syringomas.

Methods: A retrospective analysis was performed using data from medical records, routine questionnaires, and clinical photographs of 55 patients with periorbital syringoma who underwent intralesional electrosurgery. Read More

View Article

Download full-text PDF

Source
https://academic.oup.com/asj/advance-article/doi/10.1093/asj
Publisher Site
http://dx.doi.org/10.1093/asj/sjz288DOI Listing
October 2019
2 Reads

Fine-needle aspiration cytology of chondroid syringoma.

Diagn Cytopathol 2019 Dec 1;47(12):1324-1325. Epub 2019 Oct 1.

Department of Cytology and Gynecologic Pathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/dc.24317DOI Listing
December 2019
1 Read

Fusion of the Genes and in Malignant Chondroid Syringoma.

Cancer Genomics Proteomics 2019 Sep-Oct;16(5):345-351

Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.

Background/aim: Malignant chondroid syringoma is a rare tumor of unknown pathogenesis.

Materials And Methods: Genetic analyses were performed on a malignant chondroid syringoma.

Results: G-banding analysis of short-term cultured tumor cells yielded the karyotype 46,Y,t(X;6)(p11;p21)[15]/46,XY[2]. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.21873/cgp.20139DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727079PMC
January 2020
6 Reads

[Palpebral hidrocystoma].

Pan Afr Med J 2019 30;33:70. Epub 2019 May 30.

Hôpital Civil Tétouan Maroc, Centre Hospitalier Régional Tétouan, Maroc.

Palpebral hidrocystomas are benign tumors also known as cystic apocrine adenoma, cyst of sweat gland, apocrine retention cyst or cyst of Moll. They originate from eccrine or apocrine sweat glands and often occur on the face and the eyelids. Other atypical locations such as the chest, the shoulders and the foreskin have been reported. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.11604/pamj.2019.33.70.15601DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689838PMC
September 2019
5 Reads

Ln-γ 2 chain of laminin-332 is a useful marker in differentiating between benign and malignant sclerosing adnexal neoplasms.

Histopathology 2020 Jan 13;76(2):318-324. Epub 2019 Nov 13.

Department of Pathology, Fukuoka University School of Medicine and Hospital, Fukuoka, Japan.

Aims: Laminin (Ln)-γ 2, one of the chains of Ln-332, is a marker of invasive tumours and is frequently expressed as a monomer in malignant tumours. Desmoplastic trichoepithelioma (DTE), some types of basal cell carcinoma (BCC) (infiltrating and morphoeic BCC) and microcystic adnexal carcinoma (MAC) belong to a group of tumours known as sclerosing adnexal neoplasms (SAN) that are frequently difficult to differentiate and often require immunohistochemistry for diagnosis. The aim of this study was to assess the usefulness of Ln-γ 2 expression in the differential diagnosis of DTE, infiltrating/morphoeic BCC, MAC and syringoma. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/his.13974DOI Listing
January 2020
4 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

Multiple Scrotal Cysts Composed of Combined Syringomas and Epidermal Inclusion Cysts: A Previously Unreported Association.

Am J Dermatopathol 2020 Jan;42(1):52-54

Department of Pathology, Southern California Permanente Medical Group, Sunset Medical Center, Los Angeles, CA.

Epidermal inclusion cyst (EIC) and syringoma are both benign lesions that are primarily asymptomatic and occur at various places on the body. Although both EIC and syringoma are common, their joint appearance has not been previously reported. These benign proliferations target different populations, and with differing clinical presentations. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000001489DOI Listing
January 2020
3 Reads

Genital Lesions Masquerading as Condyloma Acuminata: A Case Series Report.

Iran J Public Health 2019 Jun;48(6):1161-1164

Skin Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Herein we report three married women referred to Dermatology Clinic of Loghman Hakim Hospital, Tehran, Iran in 2017 for evaluation and treatment of genital warts. Two patients were complaining of flat-topped papules on their labia major and the third one was presented with asymptomatic papillary projections on her vestibule and inner aspect of both labia minora. Histological examination revealed the diagnosis of syringoma, lymphangioma circumscriptum (LC) and vestibular papillomatosis respectively. Read More

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6635342PMC
June 2019
10 Reads

Evidence-Based Clinical Practice Guidelines for Microcystic Adnexal Carcinoma: Informed by a Systematic Review.

JAMA Dermatol 2019 Jul 3. Epub 2019 Jul 3.

Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.

Importance: Microcystic adnexal carcinoma (MAC) occurs primarily in older adults of white race/ethnicity on sun-exposed skin of the head and neck. There are no formal guiding principles based on expert review of the evidence to assist clinicians in providing the highest-quality care for patients.

Objective: To develop recommendations for the care of adults with MAC. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamadermatol.2019.1251DOI Listing
July 2019
13 Reads

Chondroid syringoma of the heel masquerading as a malignant tumour: A potential pitfall in diagnosis.

Australas J Dermatol 2020 Feb 25;61(1):60-61. Epub 2019 Jun 25.

Department of Dermatology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ajd.13097DOI Listing
February 2020
3 Reads

Multiple eruptive syringomas on the penis.

Cutis 2019 May;103(5):E15-E16

Department of Dermatology, Keck School of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California, USA.

View Article

Download full-text PDF

Source
May 2019
2 Reads

Chondroid Syringoma Mimicking Basal Cell Carcinoma.

Actas Dermosifiliogr 2020 May 25;111(4):341-343. Epub 2019 May 25.

Unidad de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario San Cecilio, Granada, España.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ad.2018.10.023DOI Listing
May 2020
7 Reads

Fine needle aspiration cytology as a preliminary diagnostic tool in chondroid syringoma: a case report and review.

Clin Cosmet Investig Dermatol 2019 5;12:209-218. Epub 2019 Apr 5.

Department of Dermatology and Venereology, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.

We report a case of chondroid syringoma (CS) in a 44-year-old male. He presented with a firm asymptomatic nodule in his left upper lip of 2-year duration. The initial clue to the diagnosis was made on fine needle aspiration cytology (FNAC), and a final diagnosis was based on histopathological examination. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2147/CCID.S195733DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497915PMC
April 2019
10 Reads

Bilateral Facial Apocrine Fibrosing Hamartoma Mimicking Microcystic Adnexal Carcinoma.

Am J Dermatopathol 2019 Oct;41(10):767-770

Dermatopathology Department, Dermatopathologie Friedrischafen/Bodensee, Friedrischafen, Germany.

An otherwise healthy 50-year-old woman was evaluated for the presence of 2 erythematous, and slightly pruritic plaques, involving both cheeks for 30 years. Left-side skin biopsy showed a diffuse proliferation of ductal structures horizontally arranged and involving the reticular dermis that resembled tubular adenoma embedded in a sclerotic stroma and surrounded by a peculiar periductal desmoplasia. Nuclear atypia or mitosis was not found. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000001433DOI Listing
October 2019
10 Reads

Benign chondroid syringoma of the orbit: an atypical location.

Orbit 2020 Apr 26;39(2):135-138. Epub 2019 Apr 26.

Oculoplastic and Reconstructive Department, Hospital Queen Elizabeth, Kota Kinabalu, Sabah, Malaysia.

A 31-year-old male with no known medical illness presented with painless left eye protrusion for the past 2 years. Radiographic features were of an extraconal superior orbital mass with no invasion of adjacent structures. The patient underwent an excisional biopsy of the left superior extraconal mass a week later. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/01676830.2019.1604766DOI Listing
April 2020
9 Reads

Comparison of microinsulated needle radiofrequency and carbon dioxide laser ablation for the treatment of syringoma.

Dermatol Ther 2019 05 2;32(3):e12912. Epub 2019 May 2.

Department of Dermatology, National Medical Center, Seoul, Republic of Korea.

Syringoma is a benign adnexal tumor originating from the intradermal eccrine ducts and predominantly occurs in women at puberty or later in life. We present a case of a 30-year-old woman with a 2-year history of syringoma on her neck and axillar region. She was treated with two devices in a split manner. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/dth.12912DOI Listing
May 2019
12 Reads

Disseminated Syringomas of the Upper Extremities in a Young Woman.

Cureus 2018 Nov 21;10(11):e3619. Epub 2018 Nov 21.

Dermatology, Clinical Pathology Associates, Austin, USA.

Syringomas are benign, eccrine sweat gland tumors frequently found on the eyelids and neck in post-pubescent women and may present in healthy individuals or be associated with various medical comorbidities. We present a case of an otherwise healthy 19-year-old female with an abrupt onset of disseminated syringomas on the bilateral forearms and dorsal hands. Eruptive acral syringomas have not been previously reported in adolescents, and this diagnosis should be considered in patients presenting with a papular eruption on the hands and forearms. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.7759/cureus.3619DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344065PMC
November 2018
6 Reads

Benign chondroid syringoma affecting the upper lip: Report of a rare case and review of literature.

J Oral Maxillofac Pathol 2018 Sep-Dec;22(3):401-405

Department of Conservative Dentistry and Endodontics, Dental College, Regional Institute of Medical Sciences, Imphal, Manipur, India.

Chondroid syringoma (CS) (mixed tumor of the skin) is a rare neoplasm of the sweat glands, which presents itself as a slow-growing, painless, nonulcerated, subcutaneous or intracutaneous mass often occurring in the head and neck region. The clinician may miss the diagnosis of this lesion due to its rarity. CS should be considered in the differential diagnosis of any subcutaneous nodules, especially in the head and neck region. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/jomfp.JOMFP_35_18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306603PMC
January 2019
8 Reads

Immunoreactivity for Sox10 in Basaloid Neoplasms of The Skin.

Appl Immunohistochem Mol Morphol 2019 02;27(2):114-118

Section of Dermatopathology, Division of Surgical Pathology-Cytopathology, University of Virginia Medical Center, Charlottesville, VA.

Basaloid tumors of the skin pose a diagnostic challenge to pathologists, because the differential diagnosis is broad, sometimes with subtle differentiating features. We evaluated SOX10 expression in 120 primary cutaneous tumors with epidermal, sweat glandular, neuroendocrine/neuroectodermal, follicular, and sebaceous lineages. Our findings were compared with those of previous studies that evaluated SOX10 in tumors of the skin. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/PAI.0000000000000721DOI Listing
February 2019
16 Reads

Cyto-Histopathological Correlation of Skin Adnexal Tumors: A Short Series.

J Cytol 2018 Oct-Dec;35(4):204-207

Department of Pathology, ESI Hospital, New Delhi, India.

Background: Skin adnexal neoplasms are relatively rare and thus uncommonly encountered in routine pathology practice.

Aims: The present study was conducted with the aim to diagnose various skin adnexal tumors on fine-needle aspiration cytology (FNAC) followed by confirmation on histopathology and immunohistochemistry of the excised tumor.

Materials And Methods: A total of 11 cases of superficial nodular swellings of the skin were studied over a period of 2 years from 2015 to 2016. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/JOC.JOC_63_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6210812PMC
December 2018
18 Reads

Hyaline Cell-Rich Apocrine Mixed Tumor with Cytologic Atypia.

Authors:
Chika Ohata

Dermatopathology (Basel) 2018 Jul-Sep;5(3):108-112. Epub 2018 Sep 13.

Department of Dermatology, Kurume University School of Medicine, Kurume, Japan.

Hyaline cell-rich apocrine mixed tumor is relatively rare, and it often possesses atypical cells. Despite the presence of atypical cells, other histopathological features such as well circumscription, smooth border, predominance of bland cells, and no mitotic figures lead to classify these tumors as benign. In addition, no recurrence or metastasis has been reported even when cytologic atypia is identified. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000492668DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180261PMC
September 2018
4 Reads

Dermoscopy of Adnexal Tumors.

Dermatol Clin 2018 Oct 16;36(4):397-412. Epub 2018 Aug 16.

Dermatology Department, Hospital General Universitario de Alicante, ISABIAL, C/Maestro Alonso 109, 03010 Alicante, Spain.

Cutaneous adnexal tumors include lesions with apocrine, eccrine, follicular, sebaceous, and mixed differentiation. Most are benign and sporadic, although malignant forms are occasionally observed and some cases develop in the setting of inherited syndromes. These tumors often cause immense diagnostic difficulty. Read More

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S07338635183107
Publisher Site
http://dx.doi.org/10.1016/j.det.2018.05.007DOI Listing
October 2018
67 Reads

Milia-like idiopathic calcinosis cutis and plaque-type syringoma in a girl with Down syndrome.

J Dermatol 2019 Apr 8;46(4):e136-e137. Epub 2018 Sep 8.

Department of Dermatology, Gunma University Graduate School of Medicine, Maebashi, Japan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/1346-8138.14635DOI Listing
April 2019
23 Reads

A Case Report of Chondroid Syringoma on the Nose in a Young Male of Middle Eastern Descent.

J Cutan Med Surg 2019 Jan/Feb;23(1):99-101. Epub 2018 Jul 24.

1 Washington University School of Medicine in St. Louis, St. Louis, MO, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1203475418791558DOI Listing
November 2019
11 Reads

A rare case of hyaline cell-rich atypical chondroid syringoma with divergent differentiation.

Indian J Pathol Microbiol 2018 Jul-Sep;61(3):428-430

Department of Pathology, Sapthagiri Institute of Medical Sciences and Research Centre, Bengaluru, Karnataka, India.

Chondroid syringoma (CS) also known as mixed tumor of the skin, is a rare benign adnexal tumor accounting for < 0.098%. Epithelial cells arranged in cords and tubules set in myxoid or chondroid stroma. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/IJPM.IJPM_101_17DOI Listing
November 2018
20 Reads

Erratum: Case of chondroid syringoma mimicking a nodular hidradenoma: A diagnostic pitfall on cytopathology.

Authors:

Diagn Cytopathol 2018 07 21;46(7):645. Epub 2018 May 21.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/dc.23973DOI Listing
July 2018
4 Reads

Penile eruptive syringoma.

Pan Afr Med J 2017;28:268. Epub 2017 Nov 28.

Medical School, Centro Universitário Barão de Mauá, Ribeirão Preto, São Paulo, Brazil.

View Article

Download full-text PDF

Source
http://www.panafrican-med-journal.com/content/article/28/268
Publisher Site
http://dx.doi.org/10.11604/pamj.2017.28.268.14437DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5989174PMC
November 2017
31 Reads

Treatment of giant vulvar syringomas with topical adelmidrol: The role of mast cells.

Australas J Dermatol 2018 Nov 4;59(4):e305-e307. Epub 2018 Jun 4.

Department of Dermatology, University General Hospital of Heraklion, Heraklion, Crete, Greece.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1111/ajd.12850
Publisher Site
http://dx.doi.org/10.1111/ajd.12850DOI Listing
November 2018
19 Reads

Malignant Mixed Tumor of the Finger: A Case Report.

J Hand Surg Asian Pac Vol 2018 Jun;23(2):286-289

* Departments of Orthopaedic Surgery, Nara Medical University, Nara, Japan.

We present a very rare case of malignant chondroid syringoma of the fingertip in a 44-year-old man that was reconstruced by neurovascular island flap after the complete tumor resection of the fingertip. Although it is a rare tumor at an unusual area, it should be included in the differential diagnosis of the finger tumors. Read More

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1142/S2424835518720190DOI Listing
June 2018
9 Reads

Multiple Papules on the Penis: Answer.

Am J Dermatopathol 2018 May;40(5):387

National Skin Centre, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/DAD.0000000000000805DOI Listing
May 2018
10 Reads

Familial eruptive syringoma.

Hong Kong Med J 2018 04;24(2):200-202

Department of Pathology, Sakarya University Training and Research Hospital, Sakarya, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.12809/hkmj144415DOI Listing
April 2018
5 Reads

Vulvar syringomas as a part of nonfamilial generalized eruptive form: Unusual lesions leading to pseudohyper-trophy of the labia majora.

Dermatol Online J 2018 Mar 15;24(3). Epub 2018 Mar 15.

Bakırköy Dr. Sadi Konuk Research & Training Hospital, Dermatology Clinic, İstanbul, Turkey.

We present a case of eruptive generalized syringoma with vulvar involvement. This case is unique in terms of being a nonfamilial, linear variant, leading to pseudohypertrophy of the labia majora. Read More

View Article

Download full-text PDF

Source
March 2018
12 Reads

Asymptomatic flesh-colored lobular nodule on the nose.

Dermatol Online J 2018 Feb 15;24(2). Epub 2018 Feb 15.

Department of Dermatology, Dicle University Medical Faculty, Diyarbakır, Turkey,.

Chondroid syringoma is a rare benign tumor of the skin appendages. Chondroid syringoma is mostly manifested by a slow-growing, painless, well defined subcutaneous or intradermal nodule. A 43-year-old man presented to our clinic with the complaint of an asymptomatic nodule on the dorsum of the nose for 8 months. Read More

View Article

Download full-text PDF

Source
February 2018
17 Reads

Chondroid syringoma with extensive cystic change and focal syringometaplasia: A rare histomorphological finding.

Indian J Pathol Microbiol 2018 Jan-Mar;61(1):143-144

Department of Pathology, All India Institute of Medical Sciences, New Delhi, India.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.4103/IJPM.IJPM_539_16DOI Listing
January 2019
3 Reads

Disseminated Asymptomatic Papules Over the Body.

JAMA Dermatol 2018 07;154(7):835-836

Department of Dermatology, Peking University First Hospital, Beijing, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamadermatol.2017.6054DOI Listing
July 2018
4 Reads