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Cytomorphology of Pleomorphic Fibroma of Skin: a Diagnostic Enigma
Case Report Cytomorphology of pleomorphic fibroma of skin: A diagnostic enigma ABSTRACT Pleomorphic fibroma (PF) is a benign, polypoid, or dome‑shaped cutaneous neoplasm with cytologically atypical fibrohistiocytic cells. We describe the cytomorphological features of PF retrospectively with histopathological diagnosis in a 38‑year‑old male who presented with 3 × 1.5 cm swelling in the soft tissues of the thigh for 6 months. This lesion is benign despite the presence of pleomorphic or bizarre cells. We review the differential diagnosis of PF with other mesenchymal tumors. To the best of our knowledge, cytomorphological features on fine needle aspiration cytology of this tumor are not yet documented in literature. Key words: Fine needle aspiration cytology; pleomorphic cells; pleomorphic fibroma. Introduction thigh. Fine needle aspiration cytology (FNAC) was done and slides were stained with Giemsa stain. The aspirate yielded Pleomorphic fibroma (PF) of the skin is a rare benign fibrous cellular smears. Background showed metachromatic stromal tumor.[1] The lesion is usually polypoid, located in the dermis, fragments. Cells were pleomorphic having very large nuclei and is formed by coarse collagen bundles with sparse cells. (monster cells) with scanty cytoplasm. Few of the nuclei It is also characterized by the presence of marked cellular showed single nucleoli [Figure 1]. Nuclear membranes atypia and pleomorphism without mitosis.[1] We describe the frequently showed notches, creases, or folds. Cells were cytomorphological features on fine needle aspiration (FNA) lying singly and occasionally forming clusters. These were smears of a histologically and immunohistochemically proven admixed with the spindle cell component along with few case of PF. -
Storiform Collagenoma: Case Report Colagenoma Estoriforme: Relato De Caso
CASE REPORT Storiform collagenoma: case report Colagenoma estoriforme: relato de caso Guilherme Flosi Stocchero1 ABSTRACT INTRODUCTION Storiform collagenoma is a rare tumor, which originates from the Storiform collagenoma or sclerotic fibroma is a rare proliferation of fibroblasts that show increased production of type-I benign skin tumor that usually affects young adults collagen. It is usually found in the face, neck and extremities, but and middle-age individuals of both sexes. This tumor is it can also appear in the trunk, scalp and, less frequently, in the slightly predominant in women. Storiform collagenoma oral mucosa and the nail bed. It affects both sexes, with a slight female predominance. It may be solitary or multiple, the latter being appears as a small papule or solid fibrous nodule. an important marker for Cowden syndrome. It presents as a painless, It is well-circumscribed, pink, whitish or skin color, solid nodular tumor that is slow-growing. It must be considered in the painless and of slow-growing. This tumor is often differential diagnosis of other well-circumscribed skin lesions, such as found in face and limbs, but it can also appears in dermatofibroma, pleomorphic fibroma, sclerotic lipoma, fibrolipoma, the chest, scalp and, rarely, in oral mucosa and nail giant cell collagenoma, benign fibrous histiocytoma, intradermal Spitz bed. Storiform collagenoma often appears as single nevus and giant cell angiohistiocytoma. tumor, and the occurrence of multiple tumors is an important indication of Cowden syndrome, which is Keywords: Collagen; Hamartoma; Skin neoplasms; Fibroma; Skin; Case a heritage genodermatosis of autosomal dominant reports condition.(1-4) Storiform collagenoma has as differential diagnosis other well-circumscribed skin tumors such RESUMO as dermatofibroma, pleomorphic fibroma, sclerotic O colagenoma estoriforme é um tumor raro originado a partir da lipoma, fibrolipoma, giant cell collagenoma, benign proliferação de fibroblastos com produção aumentada de colágeno tipo I. -
A Cutaneous Horn-Like Form of Juvenile Xanthogranuloma
Brief Report https://doi.org/10.5021/ad.2016.28.6.783 A Cutaneous Horn-Like Form of Juvenile Xanthogranuloma Young Hoon Yoon, Hyun Jeong Ju, Kyung Ho Lee, Chul Jong Park Department of Dermatology, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Korea Dear Editor: to be a cutaneous horn due to molluscum contagiosum or Juvenile xanthogranuloma (JXG) is a benign, self-healing, viral wart, and a shave biopsy was performed. non-Langerhans cell histiocytosis predominantly affecting Histopathologic examination revealed hyperkeratosis and infants and children. Usually, the clinical presentation is parakeratosis in the epidermis and dense intradermal his- characterized by solitary or multiple yellowish or red-brown tiocytic infiltrates, some of which contained foamy cells firm papules or nodules on the head, neck, and trunk1,2. and Touton giant cells (Fig. 2). Histopathological findings Herein, we report the case of a solitary JXG with an un- were consistent with a diagnosis of JXG. usual clinical presentation. JXG was first described by Adamson in 1905. Histological A 4-year-old boy presented with an asymptomatic nodule examination revealed an ill-defined, unencapsulated, on the left forearm since 2 months. The lesion was a dense histiocytic infiltration in the dermis. In mature le- corn-shaped, erythematous to yellowish nodule measuring sions, histiocytes have a foamy appearance, and Touton 0.5 cm in diameter and 0.7 cm in height. The apical part giant cells, which are characteristic of JXG, are observed. of the nodule showed marked hyperkeratosis (Fig. 1). The The clinical course tends to be benign, and lesions sponta- patient’s parents reported that it had spontaneously devel- neously regress over a period of months to years. -
8.5 X12.5 Doublelines.P65
Cambridge University Press 978-0-521-87409-0 - Modern Soft Tissue Pathology: Tumors and Non-Neoplastic Conditions Edited by Markku Miettinen Index More information Index abdominal ependymoma, 744 mucinous cystadenocarcinoma, 631 adult fibrosarcoma (AF), 364–365, 1026 abdominal extrauterine smooth muscle ovarian adenocarcinoma, 72, 79 adult granulosa cell tumor, 523–524 tumors, 79 pancreatic adenocarcinoma, 846 clinical features, 523 abdominal inflammatory myofibroblastic pulmonary adenocarcinoma, 51 genetics, 524 tumors, 297–298 renal adenocarcinoma, 67 pathology, 523–524 abdominal leiomyoma, 467, 477 serous cystadenocarcinoma, 631 adult rhabdomyoma, 548–549 abdominal leiomyosarcoma. See urinary bladder/urogenital tract clinical features, 548 gastrointestinal stromal tumor adenocarcinoma, 72, 401 differential diagnosis, 549 (GIST) uterine adenocarcinomas, 72 genetics, 549 abdominal perivascular epithelioid cell tumors adenofibroma, 523 pathology, 548–549 (PEComas), 542 adenoid cystic carcinoma, 1035 aggressive angiomyxoma (AAM), 514–518 abdominal wall desmoids, 244 adenomatoid tumor, 811–813 clinical features, 514–516 acquired elastotic hemangioma, 598 adenomatous polyposis coli (APC) gene, 143 differential diagnosis, 518 acquired tufted angioma, 590 adenosarcoma (mullerian¨ adenosarcoma), 523 genetics, 518 acral arteriovenous tumor, 583 adipocytic lesions (cytology), 1017–1022 pathology, 516 acral myxoinflammatory fibroblastic sarcoma atypical lipomatous tumor/well- aggressive digital papillary adenocarcinoma, (AMIFS), 365–370, 1026 differentiated -
Precancerous Diseases of Maxillofacial Area
PRECANCEROUS DISEASES OF MAXILLOFACIAL AREA Text book Poltava – 2017 0 МІНІСТЕРСТВО ОХОРОНИ ЗДОРОВ’Я УКРАЇНИ ВИЩИЙ ДЕРЖАВНИЙ НАВЧАЛЬНИЙ ЗАКЛАД УКРАЇНИ «УКРАЇНСЬКА МЕДИЧНА СТОМАТОЛОГІЧНА АКАДЕМІЯ» АВЕТІКОВ Д.С., АЙПЕРТ В.В., ЛОКЕС К.П. AVETIKOV D.S., AIPERT V.V., LOKES K.P. Precancerous diseases of maxillofacial area ПЕРЕДРАКОВІ ЗАХВОРЮВАННЯ ЩЕЛЕПНО-ЛИЦЕВОЇ ДІЛЯНКИ Навчальний посібник Text-book Полтава – 2017 Poltava – 2017 1 UDK 616.31-006 BBC 56.6 A 19 It is recommended by the Academic Council of the Higher state educational establishment of Ukraine "Ukrainian medical stomatological academy" as a textbook for English-speaking students of higher education institutions of the Ministry of Health of Ukraine (Protocol № 3, 22.11.2017). Writing Committee D.S. Avetikov – doctor of medicsl science, professor, chief of department of surgical stomatology and maxillo-facial surgery with plastic and reconstructive surgery of head and neck of the Higher state educational establishment of Ukraine ―Ukrainian medical stomatological academy‖. V.V. Aipert – candidate of medical science, assistant professor of department of surgical stomatology and maxillo-facial surgery with plastic and reconstructive surgery of head and neck of the Higher state educational establishment of Ukraine ―Ukrainian medical stomatological academy‖ K.P. Lokes - candidate of medical science, associate professor of department of surgical stomatology and maxillo-facial surgery with plastic and reconstructive surgery of head and neck of the Higher state educational establishment of Ukraine ―Ukrainian medical stomatological academy‖ Reviewers: R. Z. Ogonovski, doctor of medicsl science, professor, chief of department of surgical stomatology and maxillo-facial surgery ―Lviv national medical university named of D.Galicky‖. Y.P. -
Dermatopathology
Dermatopathology Clay Cockerell • Martin C. Mihm Jr. • Brian J. Hall Cary Chisholm • Chad Jessup • Margaret Merola With contributions from: Jerad M. Gardner • Talley Whang Dermatopathology Clinicopathological Correlations Clay Cockerell Cary Chisholm Department of Dermatology Department of Pathology and Dermatopathology University of Texas Southwestern Medical Center Central Texas Pathology Laboratory Dallas , TX Waco , TX USA USA Martin C. Mihm Jr. Chad Jessup Department of Dermatology Department of Dermatology Brigham and Women’s Hospital Tufts Medical Center Boston , MA Boston , MA USA USA Brian J. Hall Margaret Merola Department of Dermatology Department of Pathology University of Texas Southwestern Medical Center Brigham and Women’s Hospital Dallas , TX Boston , MA USA USA With contributions from: Jerad M. Gardner Talley Whang Department of Pathology and Dermatology Harvard Vanguard Medical Associates University of Arkansas for Medical Sciences Boston, MA Little Rock, AR USA USA ISBN 978-1-4471-5447-1 ISBN 978-1-4471-5448-8 (eBook) DOI 10.1007/978-1-4471-5448-8 Springer London Heidelberg New York Dordrecht Library of Congress Control Number: 2013956345 © Springer-Verlag London 2014 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. Exempted from this legal reservation are brief excerpts in connection with reviews or scholarly analysis or material supplied specifi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. -
Cutaneous Horn: a Potentially Malignant Entity
Letter to the editor Cutaneous horn: a potentially malignant entity Cutaneous horn: a potentially malignant entity N. F. Fernandes, S. Sinha, W. C. Lambert, and R. A. Schwartz S UMMARY A cutaneous horn is a conical, dense, hyperkeratotic protrusion that often appears similar to the horn of an animal. It is a morphologic designation referring to an unusually cohesive keratinized material, not a true pathologic diagnosis. Cutaneous horns occur in association with, or as a re- sponse to, a wide variety of underlying benign, pre-malignant, and malignant cutaneous diseases. The most important common concern is distinguishing a hyperkeratotic actinic keratosis from a cutaneous squamous cell carcinoma. Keratoacanthoma is another cause, as illustrated herein as a projective cutaneous tumor with a fingernail-like appearance. The treatment of choice for cuta- neous horns is shave excision with subsequent histopathologic evaluation to rule out underlying malignancy and to guide potential further therapy. KEYIntroduction with the characterization of cutaneous horns as a WORDS medical disorder in the late eighteenth century (2). A cutaneous horn is a conical, dense hyperkeratotic cutaneous protrusion that often resembles the horn of an Epidemiology and etiology horn, cornu animal. The earliest documented case of cutaneous cutaneum, horn, or cornu cutaneum, was that of an elderly Welsh Cutaneous horns are nodules composed of hyperkerato- woman in London who was displayed commercially compact keratin that project above the surface of sis, actinic as an anomaly of nature in 1588 (1). There were the skin. They differ from animal horns by the keratosis, several other accounts of cutaneous horns in the absence of a central bone. -
Concurrence of a Fibroma and Myxoma in an Oranda Goldfish (Carassius Auratus)
Bull. Eur. Ass. Fish Pathol., 36(6) 2016, 263 Concurrence of a fibroma and myxoma in an oranda goldfish (Carassius auratus) S. Shokrpoor1*, F. Sasani1, H. Rahmati-Holasoo2 and A. Zargar2 1 Department of Pathology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran; 2 Department of Aquatic Animal Health, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran Abstract Concurrence of fibroma and myxoma in an oranda goldfish (Carassius auratus) is described. The fish had two lesions on the dorsal region of the head and the base of the dorsal fin. Histologically, in the lesion on the head the presence of stellate and reticular cells lying in a mucoid matrix was diagnosed as a myxoma. The lesion on the base of dorsal fin was composed of mature fibrocytes producing abundant collagen in interwoven fascicles and was diagnosed as a fibroma. This is the first report of concurrence of fibroma and myxoma in a fish. Introduction Fibromas are benign neoplasms of fibrocytes 2009). Fibromas have been described in electric with abundant collagenous stroma. Myxomas catfish (Malapterurus electricus) (Stolk, 1957), are tumours of fibroblast origin distinguished southern flounder (Paralichthys lethostigma) and by their abundant myxoid matrix rich in muco- the hardhead sea catfish (Arius felis) (Overstreet polysaccharides (Goldschmidt and Hendrick, and Edwards, 1976), flathead grey mullet (Mugil 2002). Among domestic animals, fibromas have cephalus) (Lopez and Raibaut, 1981), redband been frequently described in dogs. However, parrotfish (Sparisoma aurofrenatum) (Grizzle, they are uncommon neoplasms in large animals 1983), common carp (Cyprinus carpio) (Manier (Goldschmidt and Hendrick, 2002). Fibromas et al., 1984) and goldfish (Carassius auratus) in white-tailed and mule deer (Sundberg et (Constantino et al., 1999). -
Just a Cutaneous (Keratotic) Horn?
BMJ 2019;364:l595 doi: 10.1136/bmj.l595 (Published 7 March 2019) Page 1 of 2 Endgames BMJ: first published as 10.1136/bmj.l595 on 7 March 2019. Downloaded from ENDGAMES SPOT DIAGNOSIS Just a cutaneous (keratotic) horn? Jane Wilcock general practitioner, Yvonne Savage Silverdale Medical Practice, Salford, Manchester, UK A 70 year old woman attended a dermatologist with a lesion on In this case, the speed of growth made a keratoacanthoma a the dorsum of her right hand (fig 1). It had appeared over eight possibility. However, the patient also had several risk factors weeks and was painless but unsightly. She reported good health for squamous cell cancer: age, sun exposure, past lymphoma,1 and no history of warts. Fifteen years ago, she had lymphoma past chemotherapy, and no history of warts. Other invasive treated by chemotherapy; her last treatment (biological therapy) features of squamous cell cancer relevant to this case include had finished seven years ago and she had been well since. She the lesion’s arrival over eight weeks and its wide, thick, red base had holidayed in Australia for three months at a time over the with a diameter larger than the height of the horn. About 35% 2 last three years and more recently had driven frequently from of keratotic horns are invasive squamous cell cancers. http://www.bmj.com/ northern England to the south coast while a close relative was Invasive squamous cell cancer is a non-melanotic skin ill. She said she was careful to use sunscreen. malignancy with a good prognosis but may metastasise to the lymph nodes. -
Crab-Like Appearance of Cutaneous Horns 14.6% with a Premalignant and 8.3% with a Malignant
Images in CCrab-likerab-like appearanceappearance ofof cutaneouscutaneous hornshorns Clinical Practice A 65-year-old man presented with an asymptomatic bone. No such well-formed bone is observed in pedunculated growth on the chest since two years. human horns. Cutaneous horns present as a hard, Initially nodular, verrucous growth slowly enlarged, yellowish brown protrusion, often curved and have and developed into multiple horns-like projections. circumferential ridges, which are surrounded by Cutaneous examination revealed a pedunculated either normal-appearing epidermis or an acanthotic growth measuring 3 × 3 cm on the chest, with five collarette. The height of a cutaneous horn is at least well-developed horns arising from it, appearing like half of its diameter at the base. They are usually single, a crab sitting on the chest [Figure 1]. The growth had but multiple horns may occur. They most frequently a pedicle of diameter 1 cm, withan indurated, tender occur in sun-exposed parts and are typically found base of size 1.5 × 1 cm. No regional lymphadenopathy on the face and scalp, but may also occur on the was noted. The result of systemic examination was hands, penis, eyelids, nose, chest, neck and shoulder. within normal limits. The entire lesion including the Cutaneous horn has been described overlying a indurated base was excised with an adequate margin. wide variety of benign, premalignant and malignant Histopathological examination of the excised mass conditions such as seborrheic keratoses, nevus, revealed well-differentiated squamous cell carcinoma wart, molluscum contagiosum, rhinosporidiosis, in the bases of the horns, showing superficial invasion psoriasis, lichen planus, porokeratosis, actinic in broad tongues. -
A Deep Learning System for Differential Diagnosis of Skin Diseases
A deep learning system for differential diagnosis of skin diseases 1 1 1 1 1 1,2 † Yuan Liu , Ayush Jain , Clara Eng , David H. Way , Kang Lee , Peggy Bui , Kimberly Kanada , ‡ 1 1 1 Guilherme de Oliveira Marinho , Jessica Gallegos , Sara Gabriele , Vishakha Gupta , Nalini 1,3,§ 1 4 1 1 Singh , Vivek Natarajan , Rainer Hofmann-Wellenhof , Greg S. Corrado , Lily H. Peng , Dale 1 1 † 1, 1, 1, R. Webster , Dennis Ai , Susan Huang , Yun Liu * , R. Carter Dunn * *, David Coz * * Affiliations: 1 G oogle Health, Palo Alto, CA, USA 2 U niversity of California, San Francisco, CA, USA 3 M assachusetts Institute of Technology, Cambridge, MA, USA 4 M edical University of Graz, Graz, Austria † W ork done at Google Health via Advanced Clinical. ‡ W ork done at Google Health via Adecco Staffing. § W ork done at Google Health. *Corresponding author: [email protected] **These authors contributed equally to this work. Abstract Skin and subcutaneous conditions affect an estimated 1.9 billion people at any given time and remain the fourth leading cause of non-fatal disease burden worldwide. Access to dermatology care is limited due to a shortage of dermatologists, causing long wait times and leading patients to seek dermatologic care from general practitioners. However, the diagnostic accuracy of general practitioners has been reported to be only 0.24-0.70 (compared to 0.77-0.96 for dermatologists), resulting in over- and under-referrals, delays in care, and errors in diagnosis and treatment. In this paper, we developed a deep learning system (DLS) to provide a differential diagnosis of skin conditions for clinical cases (skin photographs and associated medical histories). -
A Cutaneous Horn on the Ear
CLINICAL PRACTICE Manuel Gil-Mosquera Sergio Vano-Galvan Ruth Gómez-Guerra Pedro Jaén MD, is a family physician resident, Ramon MD, is a dermatology resident, MD, is a family physician resident, MD, PHD, is Chief, Department of y Cajal University Hospital, Madrid, Spain. Department of Dermatology, Ramon y Clinico San Carlos University Dermatology, Ramon y Cajal University [email protected] Cajal University Hospital, Madrid, Spain. Hospital, Madrid, Spain. Hospital, Madrid, Spain. A cutaneous horn on the ear associated lesions can be found at the base of a cutaneous horn, Case study both benign and malignant, including: A man, 64 years of age, retired and resident on the Spanish • squamous cell carcinoma (SCC) Mediterranean coast, without family or personal history of cutaneous tumours, requested primary medical evaluation for a lesion that had • actinic keratosis been present for a year. The lesion was located on his left ear, and had • keratoacanthoma been growing progressively, without irritation, pain or other significant • Bowen disease symptoms. No loss of weight or appetite was present. • viral warts Physical examination revealed a 2 cm exophytic mass with yellowish • seborrheic keratosis coloration on the top edge of the ear, with a hyperkeratotic surface and erythematous and infiltrated base. No cervical, submandibular or • basal cell carcinoma, and, less frequently, supraclavicular nodes were found on palpation. The remainder of the • melanoma.1–3 examination did not reveal any other abnormalities. Given the high incidence of cutaneous tumours produced by sun The patient was referred to a hospital exposure, it is fundamental that general practitioners recognise dermatology department with the these lesions in order to ensure rapid diagnostic and therapeutic clinical diagnosis of cutaneous intervention.