862 results match your criteria Syringoma


Penile eruptive syringoma.

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

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

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November 2017
2 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

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Familial eruptive syringoma.

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

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

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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

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March 2018
3 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

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February 2018
2 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.

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A Case of a Malignant Cutaneous Mixed Tumor (Chondroid Syringoma) of the Scapula Treated With Staged Margin-Controlled Excision.

Am J Dermatopathol 2018 Mar 6. Epub 2018 Mar 6.

Pathology, University of Massachusetts Medical School, Worcester, MA.

Cutaneous mixed tumor (chondroid syringoma) is the cutaneous counterpart of pleomorphic adenoma of salivary glands, comprised of both epithelial and mesenchymal components. Malignant transformation is exceptionally rare, with only a few cases reported. We report a case of a malignant cutaneous mixed tumor in an 86-year-old white man who presented with a pink indurated plaque on his left scapula. Read More

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March 2018
9 Reads

Unusual cystic lesion of the eyebrow: A case report of malignant chondroid syringoma.

J Stomatol Oral Maxillofac Surg 2018 Jun 22;119(3):232-235. Epub 2018 Feb 22.

Chirurgie maxillo-faciale, stomatologie, chirurgie orale et chirurgie plastique de la face, hospices civils de Lyon-université Claude-Bernard-Lyon 1, centre hospitalier Lyon-Sud, 165, chemin du Grand-Revoyet, 69310 Pierre-Bénite, France.

Introduction: Malignant chondroid syringomas, also known as cutaneous malignant mixed tumors, are rare neoplasms that most frequently occur on the torso or extremities of women. Here, we present an illustrated case of a facial malignant chondroid syringoma.

Materials And Methods: A 32-year-old female patient with no notable medical history presented with an approximately 1cm-wide, painless, palpably-mobile subcutaneous nodule, suggestive of a sebaceous cyst, just above the middle third of the right eyebrow. Read More

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June 2018
3 Reads

Generalized eruptive syringomas.

Dermatol Online J 2017 Sep 15;23(9). Epub 2017 Sep 15.

Department of Dermatology, State University of New York Downstate Medical Center, Brooklyn, New York.

Eruptive syringoma is a rare variant of syringoma, benign neoplasms of the eccrine sweat ducts that appear on the face, neck, chest, and axillae of predominately Asian and African American women before or during puberty [1, 2]. Lesions appear as small skin-colored or slightly pigmented, flat-topped papules [2]. The condition can be cosmetically disfiguring and difficult to treat, especially in dark-skinned patients. Read More

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September 2017

Homeobox transcriptional factor engrailed homeobox 1 is expressed specifically in normal and neoplastic sweat gland cells.

Histopathology 2018 Jun 25;72(7):1199-1208. Epub 2018 Mar 25.

Department of Human Pathology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Aims: A number of homeobox transcriptional factors are utilised as organ-specific markers in the histopathological diagnosis of neoplasms. We have screened a homeobox gene that is expressed specifically in normal sweat gland cells and is useful for the histopathological diagnosis of sweat gland neoplasms.

Methods And Results: By screening an open database resource of The Human Protein Atlas, 37 genes among the 235 homeobox transcriptional factors were found to be expressed specifically in the skin. Read More

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June 2018
7 Reads
3.45 Impact Factor

Plaque-Type Syringoma Coexisting With Basal Cell Carcinoma.

Dermatol Surg 2018 Feb 6. Epub 2018 Feb 6.

Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, Texas.

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February 2018
2 Reads

A rare large cutaneous chondroid syringoma involving a toe: A case report.

Medicine (Baltimore) 2018 Feb;97(5):e9825

PET Center, The First Affiliated Hospital, College of Medicine, Zhejiang University.

Rationale: Chondroid syringoma (CS) occurs mostly on the face and neck, and rarely occurs in the toe. Malignant CS is invasive, grows quickly, and has a high recurrence rate. The presence of a bilobed CS in 1 toe has never been reported in the literature. Read More

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February 2018

Melanoma in situ and syringoma: a rare collision tumor. Clinical-pathological report of a case.

An Bras Dermatol 2017 ;92(5 Suppl 1):101-103

Department of Dermatology. Hospital Universitari Sagrat Cor, Barcelona, Spain.

Collision or contiguous tumors, defined as two or more distinct tumors occurring at one site, are often an unexpected finding and may represent a diagnostic challenge, as clinical and histological presentations do not always coincide. Various combinations of collision tumors have been described with respect to melanocytic lesions, with the most frequently reported being the combination of nevus and basal cell carcinoma. We present an unusual case on the nose involving a melanoma in situ and a clinically-inapparent syringoma, which, to the best of our knowledge, is the first report of this combination. Read More

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March 2018
4 Reads

Malignant cutaneous mixed tumor with sebaceous differentiation.

Rom J Morphol Embryol 2017 ;58(3):977-982

Servicio de Anatomia Patologica, Hospital El Bierzo, Ponferrada, Spain;

Malignant cutaneous mixed tumor (CMT) is a very rare adnexal tumor with biphasic differentiation. In rare cases, a benign CMT (chondroid syringoma) undergoes malignant transformation. Sebaceous differentiation in a cutaneous malignant mixed tumor has not been previously reported. Read More

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January 2017
1 Read

Syringocystadenoma papilliferum combined with a tubular apocrine adenoma.

An Bras Dermatol 2017 Sep-Oct;92(5):721-723

Dermatopathology Service at the Hospital Universitário Professor Alberto Antunes - Universidade Federal de Alagoas (HUPAA-UFAL) - Maceió (AL), Brazil.

Syringocystadenoma papilliferum and tubular apocrine adenoma are rare benign sweat gland tumors. Syringocystadenoma papilliferum occurs alone or in association with other tumors. Although it is rare, the association of tubular apocrine adenoma with syringocystadenoma papilliferum developing in a sebaceous nevus on the scalp is well documented. Read More

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February 2018
3 Reads

Plaque-Type Syringoma: A Case Report.

Case Rep Dermatol 2017 Sep-Dec;9(3):190-193. Epub 2017 Oct 4.

Department of Dermatology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Syringomas are benign appendageal tumors originated from eccrine ducts. The lesions usually present as multiple small, firm papules at lower eyelids and cheeks of women. Plaque-type syringoma is an infrequent form of syringoma and to date, 12 cases have been reported. Read More

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October 2017
4 Reads

Microcystic adnexal carcinoma of the orbit mimicking pagetoid sebaceous gland carcinoma.

Orbit 2018 Jun 20;37(3):235-237. Epub 2017 Oct 20.

d Medical Director, MN Eye Hospital , Chennai , India.

Microcystic adnexal carcinoma (MAC) is a rare malignancy of sweat glands that has been reported most often on the face in the form of a cutaneous lesion, with the potential for deeper invasion. The synonyms of MAC include sclerosing sweat duct carcinoma, syringomatous carcinoma, and malignant syringoma. Clinically, MAC in the periocular area has been misdiagnosed as basal cell carcinoma, squamous cell carcinoma, or even chalazia. Read More

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June 2018
1 Read

Extensive Eruptive Syringoma After Liver Transplantation.

Acta Derm Venereol 2018 01;98(1):119-120

Department of Dermatology, Hokkaido University Graduate School of Medicine, N15 W7, Kita-ku, Sapporo 060-8638, Japan.

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January 2018
1 Read

Coexistence of eruptive syringoma and bilateral nipple vitiligo: Could there be a common immunopathogenesis?

North Clin Istanb 2017 26;4(2):195-198. Epub 2017 Aug 26.

Department of Pathology, Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey.

The rarely seen eruptive syringoma (ES) is characterized by small, skin-colored, papules. Lesions are benign; however, treatment is often unsuccessful. Recent studies have a suggested role of the autoimmune response, rather than reactive proliferation of acrosyringium in the pathogenesis of ES. Read More

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Malignant chondroid syringoma of thigh with late metastasis to lung: A very rare case report.

Indian J Pathol Microbiol 2017 Jul-Sep;60(3):418-420

Department of Surgical Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India.

Mixed/biphasic tumors include epithelial-myoepithelial tumors, pleomorphic adenoma, matrix-producing tumors, cutaneous mixed tumors such as chondroid syringoma (CS), malignant mixed tumors (carcinosarcomas), pulmonary blastomas (in lung), and many others. Morphology may show overlap between various mixed tumors. At any particular site, whether these tumors are primary or metastasis from other sites is difficult to determine, more so if primary is unknown or not disclosed. Read More

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May 2018
3 Reads

Syringocystadenoma Papilliferum of Sweat Gland of Caruncle: A Unique Case Report.

Middle East Afr J Ophthalmol 2017 Apr-Jun;24(2):103-105

Department of Ophthalmology, Himalayan Institute of Medical Sciences, Swami Rama Himalayan University, Dehradun, Uttarakhand, India.

Syringocystadenoma papilliferum (SP) is a rare benign hamartomatous malformation of skin which arises from apocrine or eccrine sweat glands. Skin of the head and neck is the usual site for this but rarely involves the eyelids. It is also called as a childhood tumor since it usually appears at birth or during puberty. Read More

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October 2017
5 Reads

Chondroid Syringoma on Face.

Arch Craniofac Surg 2016 Sep 23;17(3):173-175. Epub 2016 Sep 23.

Department of Pathology, Nowon Eulji Medical Center, Eulji University School of Medicine, Seoul, Korea.

Chondroid syringoma is a rare mixed tumor of the skin which is composed of both mesenchymal and epithelial cells. Its incidence at less than 0.1% and is frequently located on the head and neck. Read More

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September 2016
1 Read

Chondroid Syringoma: Fine-needle Aspiration Cytology of a Rare Entity at an Unusual Site.

J Clin Diagn Res 2017 Jul 1;11(7):ED06-ED07. Epub 2017 Jul 1.

Specialist, Department of Pathology, ESIC Hospital, Rohini, New Delhi, India.

Chondroid syringoma, also known as benign mixed tumour of the skin, is a rare benign adnexal tumour. It is a biphasic tumour, composed of both epithelial and mesenchymal components and constitutes <0.01% of all primary skin tumours. Read More

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July 2017
2 Reads

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

Diagn Cytopathol 2018 Jan 3;46(1):59-62. Epub 2017 Aug 3.

Department of Pathology, North Delhi Municipal Corporation Medical College and Hindu Rao Hospital, New Delhi, India.

Limited literature is available on the use of fine needle aspiration (FNA) for skin tumors. Awareness of cytological features of these lesions is important to prevent misdiagnosis. A 45-year-old male, presented with slowly growing swelling over the thigh since 4 years. Read More

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January 2018
1 Read

A Case of Eruptive Syringoma Mimicking Plane Warts.

Indian Dermatol Online J 2017 Jul-Aug;8(4):284-286

Department of Dermatology and Venereology, Pramukhswami Medical College, Karamsad, Gujarat, India.

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August 2017
1 Read

Microcystic Adnexal Carcinoma: A Review of the Literature.

Dermatol Surg 2017 Aug;43(8):1012-1016

*Division of Dermatology, Department of Internal Medicine, Washington University, St. Louis, Missouri; †Department of Pathology and Immunology, Washington University, St. Louis, Missouri.

Background: Microcystic adnexal carcinoma (MAC) is a rare, locally aggressive cutaneous neoplasm that commonly occurs on the face.

Objective: The purpose of this article is to comprehensively review the current literature on MAC pertaining to epidemiology, pathogenesis, clinical presentation, histology, immunohistochemistry, prognosis, follow-up, and treatment.

Materials And Methods: An extensive literature review was conducted using OVID MEDLINE and PubMed to identify articles relating to MAC. Read More

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August 2017
9 Reads

Chondroid Syringoma of a Cheek.

J Craniofac Surg 2017 Jul;28(5):e480-e481

Department of Plastic and Reconstructive Surgery, College of Medicine, Soonchunhyang University, Cheonan, Korea.

Chondroid syringoma is an unusual, benign skin appendageal tumor originating from the eccrine and apocrine sweat glands resembling mixed tumors of the salivary glands. It develops as a slow-enlarging, small, cutaneous nodule or mass. The lesions are usually seen in older men on head and neck. Read More

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July 2017
5 Reads

Syringoid Eccrine Carcinoma of the Foot: Report of a Rare Cutaneous Adnexal Neoplasm.

Int J Surg Pathol 2017 Oct 29;25(7):659-664. Epub 2017 May 29.

1 Hartford Hospital, Hartford, CT, USA.

Syringoid eccrine carcinoma is a rare malignant adnexal tumor that typically presents in the head and neck region. Involvement of the extremities is uncommon, with only a few cases reported in the literature. Here, we report our experience with a rare case of syringoid eccrine carcinoma occurring on the plantar surface of the right foot in a 47-year-old African American woman. Read More

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October 2017
8 Reads

A case of milium-like syringoma limited to the neck.

Australas J Dermatol 2017 May;58(2):152-154

Department of Dermatology, Kangdong Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.

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May 2017
2 Reads

Generalized eruptive syringoma with poor clinical response to systemic treatment with acitretin.

J Dtsch Dermatol Ges 2017 Mar 8;15(3):325-326. Epub 2017 Feb 8.

Department of Pathology, Medical University of Gdańsk, Poland.

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A rare association in Down syndrome: milialike idiopathic calcinosis cutis and palpebral syringoma.

Cutis 2016 Dec;98(6):E22-E23

Department of Dermatology, Faculty of Medicine, University of Harran, Turkey.

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December 2016
5 Reads

Dermoscopy of isolated syringoma of the vulva.

J Am Acad Dermatol 2017 Feb;76(2S1):S37-S39

Dipartimento di Scienze Mediche, Sezione di Dermatologia, Università di Ferrara, Ferrara, Italy.

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February 2017

Angiotropic syringomatous carcinoma.

J Cutan Pathol 2017 Apr 7;44(4):397-400. Epub 2017 Feb 7.

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

Syringomatous carcinoma (SC) is a slow-growing malignant skin tumor that usually affects the face or scalp. An 83-year-old female developed SC on the sole, a rare location. Histopathologically, numerous ducts with few keratinizing cysts were seen in the upper dermis, and cords, strands and nests with sclerotic stroma were seen in the deep dermis and subcutis. Read More

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April 2017
1 Read

Local recurrence of cutaneous mixed tumor (chondroid syringoma) as malignant mixed tumor of the thumb 20 years after initial diagnosis.

J Cutan Pathol 2017 Mar 2;44(3):292-295. Epub 2017 Feb 2.

Department of Pathology, Kaiser Permanente, Sunset Medical Center, Los Angeles, California.

Benign cutaneous mixed tumor (chondroid syringoma) is the cutaneous counterpart of the benign mixed tumor (pleomorphic adenoma) of salivary glands, consisting of both epithelial and mesenchymal elements. The incidence of cutaneous mixed tumor is rare, composing <0.01% of all primary skin tumors. Read More

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March 2017
1 Read

Periorbital Syringomas Treated With an Externally Used 1,444 nm Neodymium-Doped Yttrium Aluminum Garnet Laser.

Dermatol Surg 2017 Mar;43(3):381-388

*All authors are affiliated with the Department of Dermatology, Severance Hospital, Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea.

Background: The 1,444 nm wavelength is also well absorbed in water making it a possible setting for treatment of cystic lesions such as eccrine hydrocystomas and syringomas.

Objective: The authors aimed to investigate the efficacy of an externally used 1,444 nm neodymium-doped yttrium aluminum garnet (Nd:YAG) laser for the treatment of periorbital syringomas.

Methods And Materials: Nineteen patients with periorbital syringomas were treated twice with the externally used 1,444 nm Nd:YAG laser at 2-month intervals. Read More

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Coexistence of Adult Onset Eruptive Syringoma and Bilateral Renal Cell Carcinoma: A Case Report.

Am J Dermatopathol 2017 Jan;39(1):56-58

Departments of *Dermatology, and †Department of Pathology, Ankara Numune Training and Research Hospital, Ankara,Turkey.

Eruptive syringoma is an unusual variant of syringoma, which usually presents before or during puberty. It typically occurs in large numbers as multiple yellow-brown-colored papules, which may show spontaneous regression. Because some authors have proposed that it could present as a reactive process of eccrine ducts to an inflammatory reaction caused by an unknown trigger, the exact pathomechanism is still unclear. Read More

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January 2017
1 Read

Papular Eruptions in Adult Females.

Skin Appendage Disord 2016 Sep 30;2(1-2):14-17. Epub 2016 Apr 30.

Dermatology Clinic, Hospital do Servidor Público Municipal de São Paulo, São Paulo, Brazil.

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September 2016
6 Reads

Eruptive syringomas: unresponsiveness to oral isotretinoin.

Int J Dermatol 2017 Feb 2;56(2):e38-e39. Epub 2016 Nov 2.

Department of Dermatology, State Hospital for Skin and Venereal Diseases, Thessaloniki, Greece.

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February 2017
1 Read

Acral syringomas associated with hematological neoplasm.

Indian J Dermatol Venereol Leprol 2017 Jan-Feb;83(1):136

Department of Dermatology, Hospital of León, León, Spain.

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Evaluation of Syringomas by In Vivo Reflectance Confocal Microscopy: A Report of Two Cases.

Am J Dermatopathol 2017 Nov;39(11):845-848

*Department of Dermatology, University of São Paulo, São Paulo, Brazil; †Department of Pathology, Hospital Obrero, La Paz, Bolivia; and ‡Department of Pathology, Dental School, University of São Paulo, São Paulo, Brazil.

Syringomas are benign adnexal tumors that are characterized histologically by the presence of small solid and cystic epithelial structures in the upper half of the reticular dermis. Reflectance confocal microscopy is a noninvasive diagnostic method that enables in vivo visualization of tissues with a resolution that approximates that of conventional histopathology. The use of this method in skin imaging over the past several years has improved dermatological diagnoses, creating the potential for its wide application in such diagnoses, especially for benign and malignant skin tumors. Read More

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November 2017

Retroauricular Pleomorphic Adenoma Arising from Heterotopic Salivary Gland Tissue.

Plast Reconstr Surg Glob Open 2016 Sep 23;4(9):e1028. Epub 2016 Sep 23.

West Virginia University School of Medicine, West Virginia University, Morgantown, W.Va.; Department of Pathology, West Virginia University School of Medicine, Morgantown, W.Va.; and Division of Plastic, Reconstructive and Hand Surgery, West Virginia University School of Medicine, Morgantown, W.Va.

A 38-year-old woman is described who presented with a slowly growing mass on the posterior aspect of the left ear. Excision and histopathologic evaluation revealed a pleomorphic adenoma (PA) originating from heterotopic salivary gland tissue. Many authors have presented cases of PAs originating from ceruminous glands in the external auditory canal or of so-called chondroid syringoma originating from apocrine and eccrine sweat glands. Read More

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September 2016
3 Reads

Eccrine Duct Dilation as a Marker of Cicatricial Alopecia.

Am J Dermatopathol 2017 Sep;39(9):668-671

Departments of *Pathology, and †Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, IL; and ‡Robert H. Lurie Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL.

Background: Eccrine duct dilation (EDD) and syringoma-like sweat duct proliferation have been described as reactive changes occurring in a variety of skin conditions. However, extensive evaluation of EDD in scalp biopsies performed for alopecia has not been performed.

Methods: We retrospectively examined 129 cases of cicatricial alopecia (lichen planopilaris, central centrifugal cicatricial alopecia, and discoid lupus erythematosus) and 130 cases of noncicatricial alopecias (androgenetic alopecia, telogen effluvium, and alopecia areata) for the presence of EDD. Read More

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September 2017
4 Reads

Spiradenoma causing longitudinal splitting of the nail.

Clin Exp Dermatol 2016 Oct;41(7):754-6

Department of Pathology, All India Institute Of Medical Sciences, Patna, India.

Longitudinal splitting of the nails can occur as a result of any growth arising in the nail matrix. We present a case of a 50-year-old woman who presented with an 18-month history of longitudinal splitting of the nail on her right little finger, along with pain in the proximal nail fold region, which was extremely tender to touch. Magnetic resonance imaging revealed an intensely enhancing lesion, while colour Doppler imaging revealed hypervascularity within the mass. Read More

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October 2016
2 Reads

Erythematous papules over the neck: a diagnostic conundrum.

Dermatol Online J 2016 Aug 15;22(8). Epub 2016 Aug 15.

Department of Dermatology, Katihar Medical College, Katihar, India.

Syringomas are common appendageal neoplasms, manifested as skin-colored papules, most commonly distributed over the periorbital region. We describe a patient with syringoma localized over the neck and upper chest. Read More

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Chondroid Syringoma.

Foot Ankle Spec 2017 Apr 20;10(2):167-169. Epub 2016 Sep 20.

Grant Medical Center, Columbus, Ohio.

Chondroid syringoma is a cutaneous sweat gland tumor. Despite its relative rarity, a benign and malignant variant have been described. We present a case report of chondroid syringoma of the foot in a healthy patient. Read More

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April 2017
1 Read

An unusual presentation of chondroid syringoma.

Indian J Pathol Microbiol 2016 Jul-Sep;59(3):362-4

Department of Pathology, KPC Medical College, Kolkata, West Bengal, India.

Chondroid syringoma (CS) is a rare benign tumor of the sweat gland. It generally presents as a painless, slowly growing, subcutaneous swelling, typically located on the head and neck region. The majority of the cases develop in middle aged and elderly males. Read More

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Characteristics of Eccrine Tumors in a Tertiary Institution: A 5-Year Retrospective Study.

Skinmed 2016 1;14(3):175-80. Epub 2016 Jun 1.

Department of Pathology, Yong Loo Lin School of Medicine, National University Health System and National University of Singapore.

Eccrine tumors are adnexal tumors with a varied clinical presentation and wide histological spectrum. This study aims to consolidate data on the clinical characteristics of eccrine tumors to help improve clinical acumen and management of such tumors. Histopathological records from January 2008 to December 2012 were retrieved. Read More

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June 2016
2 Reads