RESIDENT RESOURCE CENTER POWERED by • Case Report: Masson’S Tumor • Top Resident Presentations from Cosmetic Surgery Forum 2014 • Ask an Expert: Molluscum

Total Page:16

File Type:pdf, Size:1020Kb

RESIDENT RESOURCE CENTER POWERED by • Case Report: Masson’S Tumor • Top Resident Presentations from Cosmetic Surgery Forum 2014 • Ask an Expert: Molluscum RESIDENT RESOURCE CENTER POWERED BY • Case Report: Masson’s tumor • Top Resident Presentations from Cosmetic Surgery Forum 2014 • Ask an Expert: Molluscum CASE REPORT: EXCISION OF AN INTRAVASCULAR PAPILLARY ENDOTHELIAL HYPERPLASIA By Doug Richley, DO; Christine Sickles, DO, Stephen J Plumb, DO; Jonathan Cleaver, DO, FAOCD; and Lloyd Cleaver, DO, FAOCD 37-year-old Caucasian male presented for evalu- ation of a lesion located on his left superior mucosal lip (Fig. 1). He reported that the lesion was asymptomatic and had been enlarging over a Asix-month period. He admitted to mild pain with manipu- lation. He first noticed this lesion approximately two years Figure 1. before his visit. He presented to the office wanting to have the lesion removed, secondary to him being concerned due to the fact that it has been enlarging, as well as the mild pain he experiences with manipulation. Based on the clinical presentation and history, our ini- tial differential diagnosis included venous lake, dysplastic nevus, and blue nevus. The changing nature of the lesion, as well as it being mildly tender to palpation warranted that the lesion be removed. The decision was made to perform an excisional biopsy. The defect created by the excision was approximated using 5.0 Vicryl absorbable suture. A total of four interrupted sutures were used to close the defect (Fig. 2). We instructed the patient to follow-up with his primary physician five to seven days after excision for evaluation of the wound and Figure 2. to have the sutures removed. The lesion was sent for hemo- toxylin and eosin (H & E) staining and histologic review. The DISCUSSION dermatopathology report showed a proliferation of vessels Intravascular papillary endothelial hyperplasia (IPEH) or with papillary endothelial projections (Fig. 3), consistent Masson’s tumor was first described by Pierre Masson in 1923 with the diagnosis of intravascular papillary endothelial as a neoplastic process. This was due to the proliferation of hyperplasia (IPEH) or Masson’s tumor. The benign nature endothelial cells and fibrin deposition into the vessel of the of this entity did not warrant further treatment, and the lumen that lead to obstruction and degeneration. It was later patient was advised to follow-up in one year. described as a reactive process and is now regarded as a benign, FEBRUARY 2015 PRACTICAL DERMATOLOGY 27 RESIDENT RESOURCE CENTER non-neoplastic vascular lesion that can occur post-trauma.1,2 In 1976, Clearkin and Enzinger proposed the name intravascular papillary endothelial hyperplasia (IPEH).3 The lesion may also be referred to as Masson’s lesion, Masson’s tumor, Masson’s hemangio-endotheliome vegetant intravasculaire, Masson’s pseudoangiosarcoma, intravascular angiomatosis, intravascular or extravascular papillary endothelial hyperplasia.4 Masson’s tumor occurs in both males and females, show- ing a slight female predominance with a 1.0:1.2 male to female ratio. A possible hormonal role has been suggested based on this gender difference, and local angiogenic growth factors may contribute to endothelial proliferation.5 The average age of pre- sentation is 34 years old.3 Vascular lesions are common in the oral region, but Masson’s tumor is an uncommon lesion that comprises approximately two percent of vascular tumors.2 Clinically, a Masson’s tumor presents as a single firm, papule, nodule or mass. Patients may complain of pain or tenderness.1 The lesions are red or purple in color and ranges in size from 5mm to 5cm. It typically involves the fingers, head, neck, trunk, lower extremities, and upper extremities.5 Rarely these lesion arise on mucosal mem- branes, including the upper lip, lower lip, tongue, buccal mucosa, mandibular vestibule, and angle of the mouth.6 The pathogenesis of Masson’s tumor is not completely understood, but it is thought that these lesions develop as a Figure 3. reactive process during the organization and recanalization of a thrombus. This lesion is considered to be a result from trau- tures then develop within the irregular thrombus and anasto- ma or continuous stimulation.2 In the early stage of forma- mose with adjacent vascular structures. The anastomosis and tion, endothelial cells embed themselves into the thrombus. recanalization may convert the thrombus to a mass of vascu- The endothelial cells cause a separation within the thrombus larized connective tissue and cause subendothelial vascular leading to irregular digestion by collagenase. Papillary struc- wall swelling.7 TOP 10 RESIDENT PRESENTATIONS FROM THE 2014 COSMETIC SURGERY FORUM A significant point of emphasis at Cosmetic Surgery Forum (CSF), which was most recently held in December in Las Vegas, is the education future generations of dermatologists. Residents are given the opportunity to conduct and present case studies, and every year, CSF acknowledges the top 10 presentations. The winning presentations given by dermatology residents at the 2014 CSF meeting include: 1. Kerry Shaughnessy: “A Chronic Pruritic Plaque on the Left Shoulder” 2. Amy Thorne: “The Extracutaneous Effects of Benign Stigmata” 3. Divya Shokeen: “Rhabdomyolysis in Patients on Isotretinoin Therapy” 4. David Rayhan: “Bilateral Peri-Ocular Primary Mucinous Carcinoma Treated with Mohs Micrographic Surgery” 5. Tatyana Petukhiva: “Significant Inter-rater Variability in Acne Scarring” 6. Bonita Kozma: “Hidradenitis Suppurtiva” 7. Cerrene Giordano: “Ulcerations of Striae Distensae” 8. Michael Graves: “Defining the Absorption Spectrum of Dihydroxyacetone, a Popular Sunless Tanner, Using Reflectance Photospectrometry” 9. Conor Dolehide: “An Adolescent with Solid Facial Edema (Morbihan Disease) 10. Tanya Khan: “Retained Dermal Filler Masquerading as Periorbital Edema” 28 PRACTICAL DERMATOLOGY FEBRUARY 2015 RESIDENT RESOURCE CENTER ASK AN EXPERT: MANAGING MOLLUSCUM Sheila Fallon Friedlander, MD discussed her current POWERED BY approach to the management of molluscum with host Adam Friedman, MD in a recent issue of NewDermMD. Dr. Friedlander says the first step to treating molluscum is to find out how long the child has had it, if anyone else in the family also has it, and how much treatment they’ve already tried. Explaining that many patients who present to her with this condition are typically frustrated because they’ve already been to a pediatrician and maybe even another dermatologist, she says education about the disease and treatment options is very important. Treatment advice can range from watchful waiting to treatment with cantharidin, if the patient is the right candidate. To hear more about how and when she uses cantharidin, as well as how she treats molluscum on the face, visit http://newdermmd.com/2014/12/ask-an-expert There are three different types of lesions described. The Doug Richley, DO is a first type is the primary form and it arises within an isolated Dermatology Resident, dilated blood vessel, most commonly a vein and occurs on 2nd year, Northeast the fingers, head, and neck. The secondary type is found in a Regional Medical Center/ preexisting vascular malformation, such as pyogenic granulo- ATSU, Kirksville, Missouri. ma or cavernous hemangioma and arises intramuscularly. The Christine Sickles, DO is a Traditional third type is the least common and is found extravascularly, Intern, Lewis-Gale Medical Center, and usually arises in the setting of a hematoma.3,8 The differ- Blacksburg, VA. Stephen J Plumb, DO is a ential diagnosis of benign oral lesions includes hemangioma, Dermatopathologist, Cleaver Dermatology, mucocele, pyogenic granuloma, endothelioma, and the malig- Kirksville, Missouri. Jonathan Cleaver, DO, nant neoplasms diagnosis includes angiosarcoma.5 FAOCD, FAOCD is Attending Dermatologist, Northeast Regional Histologically, Masson’s tumor is characterized by papil- Medical Center/ATSU, Kirksville, Missouri. Lloyd Cleaver, DO, lary structures with a central hypocellular hyaline core lined FAOCD is Program Director, Northeast Regional Medical Center/ by endothelial cells and associated thrombi. The histology ATSU, Kirksville, Missouri is usually distinct enough to make the diagnosis, but immu- The authors have no relevant disclosures. nohistochemical confirmation may be needed to ensure the 1. Adeoye A, Akang E, Fasina O. Orbital intravascular papillary endothelial hyperplasia in a Nigerian child: a case report and lesion is endothelial in origin. Von Willebrand factor, CD review of literature. Journal of Medical Case Reports 2012, 6:300. 31, factor XIIIa, and CD 43 are markers that can be used to 2. Akdur et al. Intravascular papillary endothelial hyperplasia: histomorphological and immunohistochemical features. 9 Diagnostic Pathology. 2013,8:167. highlight the endothelial lining. The histologic features that 3. Bolognia J, Rapini R, Jorizzo J. Dermatology: 2 Volume Set. Spain: Elsevier – Health Sciences Division, 2003. Print. 4. Choi C, Han K, Park K, Won Y, Yang J. Intravascular Papillary Endothelial Hyperplasia (Masson tumor) of the Skull: Case distinguish Masson’s tumor from angiosarcoma are a well Report and Literature Review. Journal of Korean Neurosurgery 2012, 52-54. circumscribed intravascular papillary hyperplasia, a prolifera- 5. Chung H, Jang Y, Jun J, Kim J, Kim S, Kim D, Lee S, Lee W. HIF-1α and VEGF expression correlates with thrombus remodeling in cases of intravascular papillary endothelial hyperplasia. Int J Clin Exp Pathol 2013;6(12):2912-2918. tive process that is confined to the intravascular space, and 6. Hiraki A, Iyama K, Shinohara M, Yonezawa H. Intravascular Papillary
Recommended publications
  • 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
    [Show full text]
  • Laser Dermatology
    Laser Dermatology David J. Goldberg Editor Laser Dermatology Second Edition Editor David J. Goldberg, M.D. Division of New York & New Jersey Skin Laser & Surgery Specialists Hackensack , NY USA ISBN 978-3-642-32005-7 ISBN 978-3-642-32006-4 (eBook) DOI 10.1007/978-3-642-32006-4 Springer Heidelberg New York Dordrecht London Library of Congress Control Number: 2012954390 © Springer-Verlag Berlin Heidelberg 2013 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, speci fi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on micro fi 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 speci fi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. Duplication of this publication or parts thereof is permitted only under the provisions of the Copyright Law of the Publisher’s location, in its current version, and permission for use must always be obtained from Springer. Permissions for use may be obtained through RightsLink at the Copyright Clearance Center. Violations are liable to prosecution under the respective Copyright Law. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a speci fi c statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use.
    [Show full text]
  • Expert-Level Diagnosis of Nonpigmented Skin Cancer by Combined Convolutional Neural Networks
    Supplementary Online Content Tschandl P, Rosendahl C, Akay BN, et al. Expert-level diagnosis of nonpigmented skin cancer by combined convolutional neural networks. JAMA Dermatol. Published online November 28, 2018. doi:10.1001/jamadermatol.2018.4378 eFigure. Sensitivities (Blue) and Specificities (Orange) at Different Threshold Cutoffs (Green) of the Combined Classifier Evaluated on the Validation Set eAppendix. Neural Network Training eTable 1. Complete List of Diagnoses and Their Frequencies Within the Test-Set eTable 2. Education of Users According to Their Experience Group eTable 3. Percent of Correct Prediction of the Malignancy Status for Specific Diagnoses of a CNN Using Either Close-up or Dermatoscopic Images This supplementary material has been provided by the authors to give readers additional information about their work. © 2018 American Medical Association. All rights reserved. Downloaded From: https://jamanetwork.com/ on 09/25/2021 eFigure. Sensitivities (Blue) and Specificities (Orange) at Different Threshold Cutoffs (Green) of the Combined Classifier Evaluated on the Validation Set A threshold cut at 0.2 (black) is found for a minimum of 51.3% specificity. © 2018 American Medical Association. All rights reserved. Downloaded From: https://jamanetwork.com/ on 09/25/2021 eAppendix. Neural Network Training We compared multiple architecture and training hyperparameter combinations in a grid-search fashion, and used only the single best performing network for dermoscopic and close-up images, based on validation accuracy, for further analyses. We trained four different CNN architectures (InceptionResNetV2, InceptionV3, Xception, ResNet50) and used model definitions and ImageNet pretrained weights as available in the Tensorflow (version 1.3.0)/ Keras (version 2.0.8) frameworks.
    [Show full text]
  • Aesthetic Treatment Outcomes of Capillary Hemangioma, Venous
    International Journal of Environmental Research and Public Health Article Aesthetic Treatment Outcomes of Capillary Hemangioma, Venous Lake, and Venous Malformation of the Lip Using Different Surgical Procedures and Laser Wavelengths (Nd:YAG, Er,Cr:YSGG, CO2, and Diode 980 nm) Samir Nammour 1,* , Marwan El Mobadder 1 , Melanie Namour 1 , Amaury Namour 1, Josep Arnabat-Dominguez 2 , Kinga Grzech-Le´sniak 3 , Alain Vanheusden 1 and Paolo Vescovi 4 1 Department of Dental Science, Faculty of Medicine, University of Liege, 4000 Liege, Belgium; [email protected] (M.E.M.); [email protected] (M.N.); [email protected] (A.N.); [email protected] (A.V.) 2 School of Dentistry, University of Barcelona, 08907 Barcelona, Spain; [email protected] 3 Dental Surgery Department, Medical University of Wroclaw, 50-425 Wroclaw, Poland; [email protected] 4 Department of Medicine and Surgery, University of Parma, 43121 Parma, Italy; [email protected] * Correspondence: [email protected] Received: 20 October 2020; Accepted: 20 November 2020; Published: 22 November 2020 Abstract: Different approaches with different clinical outcomes have been found in treating capillary hemangioma (CH), venous lake (VL), or venous malformations (VM) of the lips. This retrospective study aims to assess scar quality, recurrence rate, and patient satisfaction after different surgeries with different laser wavelengths. A total of 143 patients with CH or VM were included. Nd:YAG laser was used for 47 patients, diode 980 nm laser was used for 32 patients (treatments by transmucosal photo-thermo-coagulation), Er,Cr:YSSG laser was used for 12 patients (treatments by excision), and CO2 laser was used for 52 patients (treatments by photo-vaporization).
    [Show full text]
  • Contents SECTION 1 Fibrohistiocytic Tumors 1 Classification Of
    Contents SECTION 1 Fibrohistiocytic Tumors 1 Classification of Fibrohistiocytic Tumors 2 Dermatofibroma 3 Juvenile Xanthogranuloma 4 Solitary Reticulohistiocytoma and Multicentric Reticulohistiocytosis 5 Acrochordons and Pendulous Fibromas 6 Cutaneous Solitary Fibrous Tumor 7 Sclerotic Fibroma (Storiform Collagenoma) 8 Plaque-Like CD34-Positive Dermal Fibroma (Medallion-Like Dermal Dendrocyte Hamartoma) 9 Desmoplastic Fibroblastoma (Collagenous Fibroma) 10 Pleomorphic Fibroma of the Skin 11 Fibroma of Tendon Sheath 12 Giant Cell Tumor of Tendon Sheath 13 Cutaneous Myxoma 14 Superficial Acral Fibromyxoma 15 Cellular Digital Fibroma 16 Nuchal Fibroma and Gardner Syndrome–Associated Fibroma 17 Cerebriform Collagenoma Associated with Proteus Syndrome 18 Elastofibroma 19 Nodular Fasciitis, Proliferative Fasciitis, and Ischemic Fasciitis 20 Fibromatosis 21 Juvenile Hyaline Fibromatosis 22 Fibrous Hamartoma of Infancy 23 Calcifying Aponeurotic Fibroma 24 Dermatofibrosarcoma Protuberans 25 Angiomatoid Fibrous Histiocytoma 26 Plexiform Fibrohistiocytic Tumor 27 Soft Tissue Giant Cell Tumor of Low Malignant Potential 28 Inflammatory Myofibroblastic Tumor 29 Inflammatory Myxohyaline Tumor of Distal Extremities 30 Atypical Fibroxanthoma 31 Malignant Fibrous Histiocytoma 32 Fibrosarcoma 33 Epithelioid Sarcoma 34 Synovial Sarcoma 35 Alveolar Soft Part Sarcoma SECTION 2 Myofibroblastic and Muscle Tumors 36 Myofibroblasts, Muscle Cells, and Classification of Skin Proliferations with Myofibroblastic and Muscle Differentiation 37 Infantile Myofibromatosis
    [Show full text]
  • 4F1887115260be5ebf2f12a603c
    Down-Regulation of mir-424 Contributes to the Abnormal Angiogenesis via MEK1 and Cyclin E1 in Senile Hemangioma: Its Implications to Therapy Taiji Nakashima, Masatoshi Jinnin*, Tomomi Etoh, Satoshi Fukushima, Shinichi Masuguchi, Keishi Maruo, Yuji Inoue, Tsuyoshi Ishihara, Hironobu Ihn Department of Dermatology and Plastic Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan Abstract Background: Senile hemangioma, so-called cherry angioma, is known as the most common vascular anomalies specifically seen in the aged skin. The pathogenesis of its abnormal angiogenesis is still unclear. Methodology/Principal Findings: In this study, we found that senile hemangioma consisted of clusters of proliferated small vascular channels in upper dermis, indicating that this tumor is categorized as a vascular tumor. We then investigated the mechanism of endothelial proliferation in senile hemangioma, focusing on microRNA (miRNA). miRNA PCR array analysis revealed the mir-424 level in senile hemangioma was lower than in other vascular anomalies. Protein expression of MEK1 and cyclin E1, the predicted target genes of mir-424, was increased in senile hemangioma compared to normal skin or other anomalies, but their mRNA levels were not. The inhibition of mir-424 in normal human dermal microvascular ECs (HDMECs) using specific inhibitor in vitro resulted in the increase of protein expression of MEK1 or cyclin E1, while mRNA levels were not affected by the inhibitor. Specific inhibitor of mir-424 also induced the cell proliferation of HDMECs significantly, while the cell number was decreased by the transfection of siRNA for MEK1 or cyclin E1. Conclusions/Significance: Taken together, decreased mir-424 expression and increased levels of MEK1 or cyclin E1 in senile hemangioma may cause abnormal cell proliferation in the tumor.
    [Show full text]
  • Dermoscopy of Pigmented Skin Lesions (Part
    Dermoscopy of Pigmented Skin Lesions* (Part II) H. Peter Soyer,a MD; Giuseppe Argenziano,b MD; Sergio Chimenti, c MD; Vincenzo Ruocco,b MD aDepartment of Dermatology, University of Graz, Graz, Austria bDepartment of Dermatology, Second University of Naples, Naples, Italy cDepartment of Dermatology, University Tor Vergata of Rome, Rome, Italy * This CME article is partly reprinted from the Book and CD-Rom ’Interactive Atlas of Dermoscopy’ with permission from EDRA (Medical Publishing & New Media) -- see also www.dermoscopy.org Corresponding author: H. Peter Soyer, MD Department of Dermatology, University of Graz Auenbruggerplatz 8 - A-8036 Graz, Austria Phone: 0043-316-385-3235 Fax: 0043-0316-385-4957 E-mail: [email protected] Key words: dermoscopy, dermatoscopy, epiluminescence microscopy, incident light microscopy, skin surface microscopy, melanoma, pigmented skin lesions, clinical diagnosis 1 Dermoscopy is a non-invasive technique combining digital photography and light microscopy for in vivo observation and diagnosis of pigmented skin lesions. For dermoscopic analysis, pigmented skin lesions are covered with liquid (mineral oil, alcohol, or water) and examined under magnification ranging from 6x to 100x, in some cases using a dermatoscope connected to a digital imaging system. The improved visualization of surface and subsurface structures obtained with this technique allows the recognition of morphologic structures within the lesions that would not be detected otherwise. These morphological structures can be classified on
    [Show full text]
  • 2016 Posters
    POSTER PRESENTATIONS – TUESDAY, MAY 24, 2016 #1 ORAL GRANULOCYTIC SARCOMA AS FIRST MANIFESTATION OF ACUTE MYELOMONOCYTIC LEUKEMIA. A CASE REPORT AND REVIEW OF THE LITERATURE. S Titsinides, Dental School, U. of Athens, Greece, N Nikitakis, Dental School, U. of Athens, Greece M Georgaki, Dental School, U. of Athens, Greece D Maltezas, First Propaedeutic Department of Internal Medicine, Medical School, U. of Athens, Greece P Panayotidis, First Propaedeutic Department of Internal Medicine, Medical School, U. of Athens, Greece Objectives: Granulocytic sarcoma (GS or extramedullary myeloid tumor) is a rare solid tumor composed of immature cells of granulocytic lineage. GS develops in the course of acute myeloid leukemia and may affect various extramedullary sites. Only few cases of GS affecting the oral cavity have been reported. We present a rare oral GS case with an uncommon clinical presentation and summarize the clinicopathologic features of previously published cases. Clinical Presentation: A 76 year-old male presented with a buccal swelling of 1 month duration. No systemic diseases, other than diabetes and hypertension, were known. Clinical evaluation revealed a 2cm ulcerated mass with smooth contour and raised indurated borders, located on the right anterior buccal mucosa adjacent to sharped-edged teeth; extraoral swelling was also evident. Clinical differential diagnosis mainly included squamous cell carcinoma and chronic traumatic ulcer; other malignant tumors were also considered. Intervention and Outcome: A partial biopsy revealed a diffuse infiltrate by a monomorphous population of immature cells exhibiting nucleic atypia and high mitotic activity; immunohistochemical analysis showed myeloid and monocytic differentiation. Peripheral blood analysis showed elevated WBC (45000/¼l) combined with anemia and mild thrombocytopenia.
    [Show full text]
  • Axial Non-Contrast CT Head at 5Mm Collimation from Vertex Through Skull Base Without Contrast
    CT HEAD TECHNIQUE: Axial non-contrast CT head at 5mm collimation from vertex through skull base without contrast. FINDINGS: For patient’s stated age, ventricles, cerebral sulci, and basal cisterns are normal in size. No intracranial bleed or acute transcortical infarct. No focal mass, mass-effect, or midline shift. Evaluation of brainstem and posterior fossa is limited due to beam-hardening artifact. Within the limits of this exam, orbits, paranasal sinuses, and mastoids are normal. No depressed skull fracture or destructive calvarial lesions. IMPRESSION: No acute bleed or transcortical infarct. No acute intracranial findings. POINTERS • Age-commensurate cerebral atrophy or volume loss (prominent cerebral sulci) and compensatory ventricular prominence or dilatation (ventriculomegaly) • Old infarct with encephalomalacia (approaching CSF density), ex-vacuo ventricular dilation and ipsilateral wallerian degeneration (cerebral peduncle CST atrophy) • Scattered/confluent hypodensities within periventricular, subcortical, and deep white matter related to SVIC (microvascular ischemic changes) or post-inflammatory/infectious process • Centrum semiovale (above vents) or Corona radiata (around vents) • Cavum septum pellucidum (CSP)=anterior superior triangular with apex pointing post; Cavum vergae (CV)=posterior superior rectangular; CSP+CV (cavum septum pellucidum et vergae) can occur together; Cavum velum interpositum (CVI)=posterior inferior triangular with apex pointing ant • Lacunar infarct within lentiform nucleus + caudate = basal ganglia
    [Show full text]
  • Hemangioma: Review of Literature Tarun Ahuja, Nitin Jaggi, Amit Kalra, Kanishka Bansal, Shiv Prasad Sharma
    10.5005/jp-journals-10024-1440 TarunREVIEW Ahuja A etR TICLEal Hemangioma: Review of Literature Tarun Ahuja, Nitin Jaggi, Amit Kalra, Kanishka Bansal, Shiv Prasad Sharma ABSTRACT deep, compound) and the management of residual deformity. The therapeutic modalities currently available surgery Hemangiomas are tumors identified by rapid endothelial cell alone or in combination with endovascular embolization, proliferation in early infancy, followed by involution over time. All 1-3 other abnormalities are malformations resulting from anomalous intralesional injection of sclerosing agents, lasers, development of vascular plexuses. The malformations have systemic steroids. a normal endothelial cell growth cycle that affects the veins, the capillaries or the lymphatics and they do not involute. CLASSIFICATION OF HEMANGIOMAS Hemangiomas are the most common tumors of infancy and are characterized by a proliferating and involuting phase. They are Classifying vascular neoplasms has always been a challenge. seen more commonly in whites than in blacks, more in females Until recently, most classification of these neoplasms was than in males in a ratio of 3:1. based on a mixture of clinical, radiological and pathological Keywords: Hemangiomas, Tumor, Vascular malformations. features, and there was little agreement on histopathologic How to cite this article: Ahuja T, Jaggi N, Kalra A, Bansal K, classification. Some of the most accepted classifications are as: Sharma SP. Hemangioma: Review of Literature. J Contemp I. Blood vessels and lymphatics by David I Abramson Dent Pract 2013;14(5):1000-1007. follows (1962)63 Source of support: Nil • Capillary hemangioma (strawberry mark) Conflict of interest: None declared • Cavernous hemangioma • Mixed cavernous and capillary angioma INTRODUCTION • Hypertrophic or angioblastic hemangioma Hemangioma is the most common tumor in infants • Racemose hemangioma (10-12%) and the head and neck region is the most commonly • Port-wine stain or nevus vinosus involved site (60%).
    [Show full text]
  • Diode Laser Management of Primary Extranasopharyngeal Angiofibroma Presenting As Maxillary Epulis: Report of a Case and Literature Review
    healthcare Review Diode Laser Management of Primary Extranasopharyngeal Angiofibroma Presenting as Maxillary Epulis: Report of a Case and Literature Review Saverio Capodiferro 1,† , Luisa Limongelli 1,†, Silvia D’Agostino 2,* , Angela Tempesta 1 , Marco Dolci 2, Eugenio Maiorano 3 and Gianfranco Favia 1 1 Department of Interdisciplinary Medicine, University of Bari Aldo Moro, 70121 Bari, Italy; [email protected] (S.C.); [email protected] (L.L.); [email protected] (A.T.); [email protected] (G.F.) 2 Department of Medical, Oral and Biotechnological Sciences, University of Chieti Pescara, 66100 Chieti, Italy; [email protected] 3 Department of Emergency and Organ Transplantation, University of Bari Aldo Moro, 70121 Bari, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-3930246351 † These Authors equally contributed to the article. Abstract: Juvenile nasopharyngeal angiofibroma is a rare vascular neoplasm, mostly occurring in adolescent males, and representing 0.05% of all head and neck tumors. Nevertheless, it is usually recognized as the most common benign mesenchymal neoplasm of the nasopharynx. Usually, it originates from the posterolateral wall of the nasopharynx and, although histologically benign, classi- cally shows a locally aggressive behavior with bone destruction as well as spreading through natural foramina and/or fissures to the nasopharynx, nasal and paranasal cavities, spheno-palatine foramen, Citation: Capodiferro, S.; Limongelli, infratemporal fossa and, very rarely, to the cranial cavity. Extranasopharyngeal angiofibroma is L.; D’Agostino, S.; Tempesta, A.; considered a distinct entity due to older age at presentation, different localizations (outside the Dolci, M.; Maiorano, E.; Favia, G. nasopharyngeal pterygopalatine fossa) and attenuated clinical course.
    [Show full text]
  • Soft Tissue Tumors
    Soft Tissue Tumors Basic objectives for individual lesions identification and characteristics 1. Identify the cause (etiology; pathogenesis), cell or tissue of origin, and frequency (prevalence rate) 2. List the predilection GAL – Gender predilection – Age predilection – Location predilection 3. Describe the typical clinical appearance – Unusual clinical variants – Look-alike lesions (differential diagnosis) – Systemic or genetic associations – Drug, foreign material, etc. associations 4. Describe the basic microscopic features 5. Describe the usual biologic behavior (pathophysiology) – Rate and pattern of growth – Prognosis without treatment 6. State the typical treatment(s) and the prognosis for such treatment(s) 7. Describe unique variants or features (microscopic, physiologic, clinical, etc.) Irritation fibroma (fibroma, traumatic fibroma, reactive fibrous hyperplasia): 1. From acute or repeated trauma (poor healing; exuberant scar tissue) – May develop from pyogenic granuloma – Most common soft tissue mass; 3rd most common mucosal lesion in adults – Prevalence: 12 lesions/1,000 adults 2. GAL: – None (but 2x females for biopsied cases) – 4th-6th decades – Buccal, lip, tongue, gingiva 3. Smooth-surfaced, pink (normal color), painless nodule – May be pigmented (racial pigment of surface epithelium) – May have surface frictional keratosis or traumatic ulcer – Usually sessile, may be pedunculated 4. Micro: dense, avascular fibrous stroma – No capsule – Epithelium often atrophic – Small numbers of lymphocytes in fibrous stroma 5. Usually grows to <1 cm. within 6 months; minimal increase after that – May become 3-4 cm. – Does not go away – No malignant transformation 6. Treat: Conservative surgical excision 7. Unique lesion: Leaf-shaped fibroma is flat fibroma growing under a denture base – Often with small papules along the “leaf’s” edges – 6th most common mucosal lesion; prevalence = 7/1,000, with strong female predilection – Treat same as for regular irritation fibroma Giant cell fibroma (reactive fibrous hyperplasia): 1.
    [Show full text]