A Dilated Pore of Winer with Four Openings Ru-Zhi Zhang1 and Wen-Yuan Zhu*,2
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ASCP. Cutaneous Adnexal Neoplasms: Classification and A
1355 Cutaneous Adnexal Neoplasms: Classification And A Practical Diagnostic Approach David S. Cassarino, MD, PhD, FASCP WEEKEND OF PATHOLOGY AMERICAN SOCIETY FOR CLINICAL PATHOLOGY 33 W Monroe Ste 1600 Chicago, IL 60603 Program Content and Disclosure The primary purpose of this activity is educational and the comments, opinions, and/or recommendations expressed by the faculty or authors are their own and not those of the ASCP. There may be, on occasion, changes in faculty and program content. In order to ensure balance, independence, objectivity, and scientific rigor in all its educational activities, and in accordance with ACCME Standards, the ASCP requires all individuals in positions to influence and/or control the content of ASCP CME activities to disclose whether they do or do not have any relevant financial relationships with proprietary entities producing health care goods or services that are discussed in the CME activities, with the exemption of non-profit or government organizations and non-health care related companies. These relationships are reviewed and any identified conflicts of interest are resolved prior to the activity. Faculty are asked to use generic names in any discussion of therapeutic options, to base patient care recommendations on scientific evidence, and to base information regarding commercial products/services on scientific methods generally accepted by the medical community. All ASCP CME activities are evaluated by participants for the presence of any commercial bias and this input is utilized for subsequent CME planning decisions. The individuals below have responded that they have no relevant financial relationships with commercial interests to disclose: Course Faculty: David S. -
Adnexal Tumours of the Skin J Clin Pathol: First Published As 10.1136/Jcp.44.7.543 on 1 July 1991
J Clin Pathol 199 1;44:543-548 543 Troublesome tumours 1: Adnexal tumours of the skin J Clin Pathol: first published as 10.1136/jcp.44.7.543 on 1 July 1991. Downloaded from D Cotton Introduction these are very unusual,6 and the confusion due Most adnexal tumours are benign and, if com- to the term "cylindroma" being used for a pletely excised, cause no further concern. It different, malignant, tumour of other sites may therefore be thought that there is little causes considerable difficulty. Again, duct dif- need for further subclassification. The major ferentiation is CEA positive, but the bulk of arguments for considering them further can tumour cells in all these tumours (poromas, be summarised as follows: (1) if you are not spiradenomas, and cylindromas) are CEA sure what it is, it may be something else; (2) negative. All of the above mentioned tumours clinical associations with specific subtypes will have features reminiscent of the sweat gland not become apparent if the lesions are never on electron microscopical examination and subtyped; and (3) there is academic and obses- they stain variably positive with middle sional satisfaction to be derived from weight cytokeratin antibodies such as PKKI meticulously identifying lesions as accurately and are negative for CAM5 2, S100, epithelial as possible. membrane antigen (EMA) and human milk Given these justifications I will comment on fat globule 1 (HMFG 1). what I consider to be useful and interesting Poroma, spiradenoma, and cylindroma are aspects of certain adnexal tumours. The first all derived from the outer cells of the duct and division is into tumours showing affinity with behave as benign "epitheliomas" or eccrine glands and those showing affinity with "basalomas" as these terms are variously used the pilosebaceous system. -
JMSCR Vol||08||Issue||02||Page 566-568||February 2020
JMSCR Vol||08||Issue||02||Page 566-568||February 2020 http://jmscr.igmpublication.org/home/ ISSN (e)-2347-176x ISSN (p) 2455-0450 DOI: https://dx.doi.org/10.18535/jmscr/v8i2.98 Dilated Pore of Winer Mimicking Trichofolliculoma Authors Dr J.Harshini1, Dr M.S.Srinivasan2 1Junior Resident, 2Head of the Department Department of Dermatology, Venereology and Leprosy, Chettinad Hospital and Research Institute, Kelambakkam *Corresponding Author Dr J. Harshini Junior resident, Department of Dermatology, Venereology and Leprosy, Chettinad Hospital and Research Institute, Kelambakkam Abstract Dilated pore of Winer which was originally designated as a secondary or acquired trichoepithelioma by Winer, represents an appendageal tumor with differentiation towards follicular structures. It is clinically characterised by having the appearance of a large comedone filled with keratinous material. To the best of our knowledge, there has been no report of dilated pore with a terminal hair in the centre. We herein describe such a case. Keywords: Dilated pore, Winer, Appendageal tumor, Trichoepithelioma. Introduction Case Report Dilated pore of Winer was first described by A 21 year old female presented with an Winer in 1954[1]. It is a commonly occurring asymptomatic slow growing swelling on her benign adnexal tumor of follicular neck for preceding six months. There was no differentiation[3][4]. It is commonly located on systemic symptoms and no history of similar head and neck, however dilated pore of Winer illness in the family. can also be found on the trunk of middle aged On examination a solitary skin coloured, shiny, and elderly individuals. These clinically present firm and non-tender papule was seen above the as an asymptomatic solitary enlarged pore with a right Clavicle [Figure 1]. -
Congenital Trichofolliculoma: a Very Rare Presentation
Volume 26 Number 7| Jul 2020| Dermatology Online Journal || Photo Vignette 26(7):13 Congenital trichofolliculoma: a very rare presentation Mohamed HM El-Komy MD, Heba A Abdelkader MD Affiliations: Department of Dermatology, Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt Corresponding Author: Heba A. Abdelkader MD, Mailing address: Dermatology Department, Kasr Al Aini Hospital, Cairo University, Kasr Al Aini Street, Cairo, Egypt 11562, Tel: 20-1222868716, Email: [email protected] follicular cavity with radially arranged hair follicles in Abstract different stages of development consistent with Trichofolliculoma is an uncommon hair follicle trichofolliculoma (Figure 2). hamartoma. It usually appears during adulthood on the face or scalp as a single, asymptomatic, skin- colored papule/nodule with small protruding hairs. Case Discussion Histopathological features are diagnostic. Very rare congenital cases have been reported. Herein, we Trichofolliculoma is a rare hair follicle report a congenital trichofolliculoma in a 15-year-old hamartoma/tumor. It is considered by most authors girl. to be a hamartoma rather than a neoplasm as it has all components of the hair follicle in an aberrant distribution [4]. Its differentiation is midway between Keywords: trichofolliculoma, congenital, hair follicle a hair follicle nevus and a trichoepithelioma [5]. It tumors, hamartoma usually presents in adulthood as a single lesion on the face especially around the nose. However, it is reported to occur in other sites such as the external Introduction auditory meatus, intranasal area, genitalia, lip, and Trichofolliculoma is an uncommon hair follicle vulva [6]. Rare cases of congenital trichofolliculoma hamartoma. It usually appears during adulthood on have been reported in the literature [7-11]. -
Subcutaneous Nodule on the Chest
DERMATOPATHOLOGY DIAGNOSIS Subcutaneous Nodule on the Chest Elizabeth L. Bisbee, MD; Eric W. Rudnick, MD; Vladimir Vincek, MD, PhD Eligible for 1 MOC SA Credit From the ABD This Dermatopathology Diagnosis in our print edition is eligible for 1 self-assessment credit for Maintenance of Certification from the American Board of Dermatology (ABD). After completing this activity, diplomates can visit the ABD website (http://www.abderm.org) to self-report the credits under the activity title “Cutis Dermatopathology Diagnosis.” You may report the credit after each activity is completed or after accumulating multiple credits. A healthy 45-year-old man presented to the dermatology clinic with a slow-growing subcutane- ous nodule on the left chest that had been present for years. copy THE BEST DIAGNOSIS IS: a. basal cell carcinoma b. cystic panfolliculoma c. dilated pore of Winer d. folliculosebaceousnot cystic hamartoma e. trichoblastoma PLEASE TURN TO PAGE 39 FOR THE DIAGNOSIS H&E, original magnification ×40. Do CUTIS H&E, original magnification ×600. From the Department of Dermatology, University of Florida College of Medicine, Gainesville. The authors report no conflict of interest. Correspondence: Elizabeth L. Bisbee, MD, Department of Dermatology, University of Florida College of Medicine, 4037 NW 86th Terrace, 4th Floor, Gainesville, FL 32606 ([email protected]). doi:10.12788/cutis.0293 30 I CUTIS® WWW.MDEDGE.COM/DERMATOLOGY Copyright Cutis 2021. No part of this publication may be reproduced, stored, or transmitted without the prior written permission of the Publisher. DERMATOPATHOLOGY DIAGNOSIS DISCUSSION THE DIAGNOSIS: Cystic Panfolliculoma anfolliculoma is a rare tumor of follicular origin.1 were observed (quiz image [top]). -
TP53 Abnormalities and MMR Preservation in 5 Cases of Proliferating Trichilemmal Tumours
Article TP53 Abnormalities and MMR Preservation in 5 Cases of Proliferating Trichilemmal Tumours Raquel Martín-Sanz 1, José María Sayagués 2 , Pilar García-Cano 3, Mikel Azcue-Mayorga 4, María del Carmen Parra-Pérez 2, María Ángeles Pacios-Pacios 2, Enric Piqué-Durán 5,* and Jorge Feito 2,6,* 1 Ophthalmology Department, Complejo Asistencial Universitario de Salamanca, 37007 Salamanca, Spain; [email protected] 2 Pathology Department, Complejo Asistencial Universitario de Salamanca, 37007 Salamanca, Spain; [email protected] (J.M.S.); [email protected] (M.d.C.P.-P.); [email protected] (M.Á.P.-P.) 3 Plastic Surgery Department, Complejo Asistencial Universitario de Salamanca, 37007 Salamanca, Spain; [email protected] 4 Pathology Department, Hospital José Molina Orosa, 35500 Arrecife, Spain; [email protected] 5 Dermatology Department, Hospital José Molina Orosa, 35500 Arrecife, Spain 6 Human Anatomy and Histology Department, Universidad de Salamanca, 37007 Salamanca, Spain * Correspondence: [email protected] (E.P.-D.); [email protected] (J.F.) Abstract: Proliferating trichilemmal tumours (PTT) are defined by a benign squamous cell prolifera- tion inside a trichilemmal cystic (TC) cavity. A possible explanation of this proliferative phenomenon within the cyst may be molecular alterations in genes associated to cell proliferation, which can be induced by ultraviolet radiation. Among other genes, alterations on TP53 and DNA mismatch Citation: Martín-Sanz, R.; Sayagués, repair proteins (MMR) may be involved in the cellular proliferation observed in PTT. Based on this J.M.; García-Cano, P.; Azcue-Mayorga, assumption, but also taking into account the close relationship between the sebaceous ducts and the M.; Parra-Pérez, M.d.C.; Pacios-Pacios, M.Á.; Piqué-Durán, E.; external root sheath where TC develop, a MMR, a p53 expression assessment and a TP53 study were Feito, J. -
February 2010 MONTHLY EDUCATIONAL CONFERENCE
Chicago Dermatological Society February 2010 MONTHLY EDUCATIONAL CONFERENCE Program Information Continuing Medical Education Certification and Case Presentations Wednesday, February 17, 2010 Donald E. Stephens Convention Center Rosemont, IL Conference Host: Division of Dermatology Stroger Cook County Hospital Chicago, Illinois Program Venue Information STEPHENS CONVENTION CENTER 5555 N. River Road; Rosemont, IL Registration – Ballroom 1, First Floor, Conference Center • Committee meetings • Slide & poster viewing • Lectures, business meeting & case discussions • Lunch • Exhibitors Committee Meetings 8:00 a.m. CDS Plans & Policies Committee 9:00 a.m. IDS Board of Directors Program Activities 9:00 a.m. Registration for all attendees Outside Ballroom #1, first floor of the Conference Center 9:00 a.m. - 10:00 a.m. RESIDENT LECTURE – Ballroom #2 “Problem Psoriasis” – Mark Lebwohl, MD 9:30 a.m. - 10:45 a.m. CLINICAL ROUNDS Poster viewing – Ballroom #14 Slide viewing – Ballroom #14 10:45 a.m. - 11:45 a.m. GENERAL SESSION - Ballroom #2 Sidney Barsky Lecture: “Great Cases” – Mark Lebwohl, MD 11:45 a.m. - 12:15 p.m. Lunches & visit with exhibitors 12:15 p.m. - 12:30 p.m. CDS Business meeting – Ballroom #2 12:30 p.m. - 2:30 p.m. Case Discussions – Ballroom #2 Moderator: Warren Piette, MD; Chair, Department of Dermatology; Stroger/Cook County Hospital Cases presented by Stroger/CCH Residents 2:30 p.m. Meeting adjourns Next meeting – Wednesday, April 21, 2010; Stephens Convention Center, Rosemont Future Meeting Schedule – check the CDS meeting calendar on our website: www.ChicagoDerm.org Guest Speaker Sidney Barsky Lecture Mark Lebwohl, MD Professor and Chairman, Department of Dermatology, The Mount Sinai School of Medicine; New York, NY Dr. -
Boards Fodder Hyperplasias and Benign Neoplasms of Adnexal Origin by Kristy Charles, MD, and Emily Smith, MD
boards fodder Hyperplasias and Benign Neoplasms of Adnexal Origin By Kristy Charles, MD, and Emily Smith, MD Follicular Entities Clinical Presentation Pathology Associations & Notes Basaloid follicular Nonspecific skin- Strands of basaloid cells with • PTCH mutation hamartoma colored papule numerous epidermal connections. • The familial form is autosomal More pink than BCC with no cleft- dominant and associated with milia, ing. comedones, hyperpigmented pap- ules, hypotrichosis, hypohidrosis, and palmar pits. Dilated pore of Papule with central Large cystic follicle with small Winer pore on face of elderly squamous buds. Pilar sheath acanthoma has thicker projecting Pilar sheath acan- Papule with central fingers. thoma pore on upper lip of middle aged to elderly patient Trichofolliculoma Small, papule or nod- Multiple “baby” follicles empty- ule with tuft of hair ing into a central large “mother” at central pore on the follicle. face, scalp or upper trunk. Fibrofolliculoma Central follicle with radiating thin • Birt-Hogg-Dubé syndrome: Auto- Small, skin-colored epithelial strands in a fibrovascu- somal dominant, folliculin mutation to white papules on lar stroma. (Mtor pathway). Colonic polyposis, head, neck, or upper spontaneous pneumothorax, renal Trichodiscoma trunk. Fibrofolliculoma cut in a plane cell carcinoma, medullary thyroid that does not show epithelial carcinoma. strands. Only see fibrovascular stroma. Trichoblastoma Solitary, brown or Dermal basaloid nodules in scle- • #1 tumor to grow in a nevus seba- blue-black nodule on rotic stroma. Papillary mesenchy- ceous scalp. mal bodies. Trichoepithelioma Skin-colored papule(s) Islands of basaloid cells in the • Brooke-Spiegler syndrome and mul- on nose, upper lips or upper dermis within fibrous tiple familial trichoepitheliomas cheeks. -
Simple Approach to Histological Diagnosis of Common Skin Adnexal Tumors
Journal name: Pathology and Laboratory Medicine International Article Designation: REVIEW Year: 2017 Volume: 9 Pathology and Laboratory Medicine International Dovepress Running head verso: Alhumidi Running head recto: Histological diagnosis of common skin adnexal tumors open access to scientific and medical research DOI: http://dx.doi.org/10.2147/PLMI.S139767 Open Access Full Text Article REVIEW Simple approach to histological diagnosis of common skin adnexal tumors Ahmed A Alhumidi Abstract: Most adnexal neoplasms are uncommonly encountered in routine practice, and pathologists can recognize a limited number of frequently encountered tumors. In this review, Department of Pathology, College of Medicine, King Saud University, I provide a simplified histological approach to be used by general pathologists and residents Riyadh, Saudi Arabia of pathology and dermatology programs. These tumors are classified into 1) tumors connected to epidermis, 2) tumors not connected to epidermis, 3) sebaceous tumors, and 4) dermal cysts. Keywords: skin, adnexal tumors, histology, approach Introduction Tumors of the skin appendages have been classified into four groups that exhibit histologic For personal use only. features analogous to hair follicles, sebaceous glands, apocrine glands, and eccrine glands (Figure 1). Most adnexal neoplasms are relatively uncommonly encountered in routine practice, and pathologists can recognize a limited number of frequently encountered tumors. In this article, I reviewed the histological features of the common skin adnexal tumors with an emphasis on simple diagnostic histological approach. This approach depends generally on the location of the tumor, cell cytoplasm and color of the tumor in a low power. Some tumors are located superficially and predominantly connect to epidermis and others lie deep in the dermis. -
Malignant Transformation Within Benign Adnexal Skin Tumours
Histopathology 2004, 45, 162–170 Malignant transformation within benign adnexal skin tumours B Liegl, S Leibl, M Okcu, C Beham-Schmid & S Regauer Institute of Pathology, Medical University of Graz, Graz, Austria Date of submission 21 July 2003 Accepted for publication 23 December 2003 Liegl B, Leibl S, Okcu M, Beham-Schmid C & Regauer S (2004) Histopathology 45, 162–170 Malignant transformation within benign adnexal skin tumours Aims: To report five malignant trichogenic tumours encapsulated. There was a residual benign tumour arising in longstanding, previously benign adnexal component and morphological signs such as bone neoplasms through malignant transformation. Malig- formation, dystrophic calcification and sclerosis sug- nant trichogenic adnexal tumours are extremely rare gesting long duration of the lesions. All patients except neoplasms. for one, who refused further clinical investigation due Methods and results: The patients were between to her advanced age of 79 years, had an underlying 55 years and 79 years of age. Three of the tumours systemic malignancy. were located on the arms, two on the face. Three of our Conclusions: The growth stimulus in these benign patients had a history of chronic lymphocytic leukae- adnexal neoplasms resulting in malignant transforma- mia, one patient had a history of colonic adenocar- tion may be attributed to the acquisition of additional cinoma. The duration of the tumour nodules was genetic events or to immunosuppression due to an reported as between 20 and 40 years before sudden underlying neoplastic disease. Therefore, patients with changes occurred. These changes included rapid systemic diseases or malignancy should be carefully growth, pain, itching, ulceration and bleeding. -
Like Hair Follicle Neoplasias Lixin Kan1*†, Yijie Liu1†, Tammy L Mcguire1, Michael a Bonaguidi2,3 and John a Kessler1
Kan et al. Journal of Biomedical Science 2011, 18:92 http://www.jbiomedsci.com/content/18/1/92 RESEARCH Open Access Inhibition of BMP signaling in P-Cadherin positive hair progenitor cells leads to trichofolliculoma- like hair follicle neoplasias Lixin Kan1*†, Yijie Liu1†, Tammy L McGuire1, Michael A Bonaguidi2,3 and John A Kessler1 Abstract Background: Skin stem cells contribute to all three major lineages of epidermal appendages, i.e., the epidermis, the hair follicle, and the sebaceous gland. In hair follicles, highly proliferative committed progenitor cells, called matrix cells, are located at the base of the follicle in the hair bulb. The differentiation of these early progenitor cells leads to specification of a central hair shaft surrounded by an inner root sheath (IRS) and a companion layer. Multiple signaling molecules, including bone morphogenetic proteins (BMPs), have been implicated in this process. Methods: To further probe the contribution of BMP signaling to hair follicle development and maintenance we employed a transgenic mouse that expresses the BMP inhibitor, Noggin, to disrupt BMP signaling specifically in subset of hair follicle progenitors under the control of neuron specific enolase (Nse) promoter. We then studied the skin tumor phenotypes of the transgenic mice through histology, immunohistochemistry and Western Blotting to delineate the underlying mechanisms. Double transgenic mice expressing BMP as well as noggin under control of the Nse promoter were used to rescue the skin tumor phenotypes. Results: We found that the transgene is expressed specifically in a subpopulation of P-cadherin positive progenitor cells in Nse-Noggin mice. Blocking BMP signaling in this cell population led to benign hair follicle-derived neoplasias resembling human trichofolliculomas, associated with down-regulation of E-cadherin expression and dynamic regulation of CD44. -
29 Epidermal Nevi, Neoplasms, and Cysts
W2921-29.qxd 18/8/05 11:27 AM Page 603 CHAPTER 29 Epidermal Nevi, Neoplasms, and Cysts EPIDERMAL NEVI follow the lines of Blaschko. The term ichthyosis hystrix Keratinizing epidermal nevi are described by a great variety had been used to describe cases with extensive bilateral of terms, such as hard nevus of Unna, soft epidermal nevus, involvement. nevus verrucosus (verrucous nevus), nevus unius lateris, The histologic changes in the epidermis are hyperplastic linear epidermal nevus, and ichthyosis hystrix. Hyper- and affect chiefly the stratum corneum and stratum malpighii. keratosis without cellular atypia characterizes them all: There is variable hyperkeratosis, acanthosis, and papilloma- melanocytic nevus cells do not occur. In some cases the tosis. Up to 62% of biopsies of epidermal nevi have this primary constituent is hyperplasia of an adnexal component pattern. About 16% show epidermolytic hyperkeratosis. At (nevus comedonicus, nevus sebaceous). These lesions are all times, other histologic patterns may be found, including a considered to represent somatic mosaicism in the affected psoriatic type, an acrokeratosis verruciformis-like type, and a region. The histologic features are apparently a consequence Darier disease-like type. of the genetic mutation affecting that region. These lesions Rarely keratinocytic and adnexal malignancies occur in follow the lines of Blascko rather than dermatomes, suggest- epidermal nevi. Any newly appearing lesion within a stable ing they represent mutations that occurred at some post- epidermal nevus should be biopsied to exclude this possi- zygotic time during fetal development. Epidermal nevi are bility. Management of epidermal nevi is difficult, since unless relatively common, with a prevalence of about 1 in 1000.