Pleomorphic Adenoma of Buccal Mucosa: a Rare Case Report
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Clinical Utility of in Situ Hybridization Assays in Head and Neck Neoplasms
Head and Neck Pathology (2019) 13:397–414 https://doi.org/10.1007/s12105-018-0988-1 INVITED REVIEW Clinical Utility of In Situ Hybridization Assays in Head and Neck Neoplasms Peter P. Luk1 · Christina I. Selinger1 · Wendy A. Cooper1,2,3 · Annabelle Mahar1 · Carsten E. Palme2,4 · Sandra A. O’Toole5,6 · Jonathan R. Clark2,4 · Ruta Gupta1,2 Received: 1 September 2018 / Accepted: 15 November 2018 / Published online: 22 November 2018 © Springer Science+Business Media, LLC, part of Springer Nature 2018 Abstract Head and neck pathology present a unique set of challenges including the morphological diversity of the neoplasms and presentation of metastases of unknown primary origin. The detection of human papillomavirus and Epstein–Barr virus associated with squamous cell carcinoma and newer entities like HPV-related carcinoma with adenoid cystic like features have critical prognostic and management implications. In salivary gland neoplasms, differential diagnoses can be broad and include non-neoplastic conditions as well as benign and malignant neoplasms. The detection of specific gene rearrange- ments can be immensely helpful in reaching the diagnosis in pleomorphic adenoma, mucoepidermoid carcinoma, secretory carcinoma, hyalinizing clear cell carcinoma and adenoid cystic carcinoma. Furthermore, molecular techniques are essential in diagnosis of small round blue cell neoplasms and spindle cell neoplasms including Ewing sarcoma, rhabdomyosarcoma, synovial sarcoma, biphenotypic sinonasal sarcoma, dermatofibrosarcoma protuberans, nodular fasciitis and inflammatory myofibroblastic tumor. The detection of genetic rearrangements is also important in lymphomas particularly in identifying ‘double-hit’ and ‘triple-hit’ lymphomas in diffuse large B cell lymphoma. This article reviews the use of in situ hybridization in the diagnosis of these neoplasms. -
Increased Mast Cell Counts in Benign and Malignant Salivary Gland Tumors
Journal of Dental Research, Dental Clinics, Dental Prospects Original Article Increased Mast Cell Counts in Benign and Malignant Salivary Gland Tumors Zohreh Jaafari-Ashkavandi1* • Mohammad-Javad Ashraf 2 1Associate Professor, Department of Oral and Maxillofacial Pathology, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran 2Associate Professor, Department of Pathology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran *Corresponding Author; E-mail: [email protected] Received: 28 October 2012; Accepted: 12 December 2013 J Dent Res Dent Clin Dent Prospect 2014;8(1):15-20 | doi: 10.5681/joddd.2014.003 This article is available from: http://dentistry.tbzmed.ac.ir/joddd © 2014 The Authors; Tabriz University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background and aims. Mast cells are one of the characteristic factors in angiogenesis, growth, and metastatic spread of tumors. The distribution and significance of mast cells in many tumors have been demonstrated. However, few studies have evaluated mast cell infiltration in salivary gland tumors. In this study, mast cell counts were evaluated in benign and malig- nant salivary gland tumors. Materials and methods. This descriptive and cross-sectional study assessed 30 cases of pleomorphic adenoma, 13 cases of adenoid cystic carcinoma, 7 cases of mucoepidermoid carcinoma (diagnosed on the basis of 2005 WHO classifica- tion), with adequate stroma in peritumoral and intratumoral areas, and 10 cases of normal salivary glands. -
Soft Tissue Cytopathology: a Practical Approach Liron Pantanowitz, MD
4/1/2020 Soft Tissue Cytopathology: A Practical Approach Liron Pantanowitz, MD Department of Pathology University of Pittsburgh Medical Center [email protected] What does the clinician want to know? • Is the lesion of mesenchymal origin or not? • Is it begin or malignant? • If it is malignant: – Is it a small round cell tumor & if so what type? – Is this soft tissue neoplasm of low or high‐grade? Practical diagnostic categories used in soft tissue cytopathology 1 4/1/2020 Practical approach to interpret FNA of soft tissue lesions involves: 1. Predominant cell type present 2. Background pattern recognition Cell Type Stroma • Lipomatous • Myxoid • Spindle cells • Other • Giant cells • Round cells • Epithelioid • Pleomorphic Lipomatous Spindle cell Small round cell Fibrolipoma Leiomyosarcoma Ewing sarcoma Myxoid Epithelioid Pleomorphic Myxoid sarcoma Clear cell sarcoma Pleomorphic sarcoma 2 4/1/2020 CASE #1 • 45yr Man • Thigh mass (fatty) • CNB with TP (DQ stain) DQ Mag 20x ALT –Floret cells 3 4/1/2020 Adipocytic Lesions • Lipoma ‐ most common soft tissue neoplasm • Liposarcoma ‐ most common adult soft tissue sarcoma • Benign features: – Large, univacuolated adipocytes of uniform size – Small, bland nuclei without atypia • Malignant features: – Lipoblasts, pleomorphic giant cells or round cells – Vascular myxoid stroma • Pitfalls: Lipophages & pseudo‐lipoblasts • Fat easily destroyed (oil globules) & lost with preparation Lipoma & Variants . Angiolipoma (prominent vessels) . Myolipoma (smooth muscle) . Angiomyolipoma (vessels + smooth muscle) . Myelolipoma (hematopoietic elements) . Chondroid lipoma (chondromyxoid matrix) . Spindle cell lipoma (CD34+ spindle cells) . Pleomorphic lipoma . Intramuscular lipoma Lipoma 4 4/1/2020 Angiolipoma Myelolipoma Lipoblasts • Typically multivacuolated • Can be monovacuolated • Hyperchromatic nuclei • Irregular (scalloped) nuclei • Nucleoli not typically seen 5 4/1/2020 WD liposarcoma Layfield et al. -
Pleomorphic Adenoma of Nasal Septum Masquerading As Squamous Cell Carcinoma: About One Case
ISSN: 2572-4193 Smail. J Otolaryngol Rhinol 2020, 6:089 DOI: 10.23937/2572-4193.1510089 Volume 6 | Issue 3 Journal of Open Access Otolaryngology and Rhinology CASE REPORT Pleomorphic Adenoma of Nasal Septum Masquerading as Squamous Cell Carcinoma: About One Case Kharoubi Smail* Check for ENT Department, Faculty of Medicine, University of Badji Mokhtar, Algeria updates *Corresponding author: Kharoubi Smail, ENT Department, Faculty of Medicine, University of Badji Mokhtar, Annaba 23000, Algeria sion. Nasal endoscopy shows a gray mass obstructing Abstract the right nasal fossa with septal deviation from left side. Pleomorphic adenoma is one of the most common benign There are no cervical lymph nodes. tumors of the major salivary glands. It can also occur in the minor salivary glands, which exist in the nasal cavity. We Computed tomography (CT) of nasal cavity and para- present a case of pleomorphic adenoma masquerading as nasal sinuses show’s a mass with tissue density and bad squamous cell carcinoma in 61-year-old man. This patient presented with nasal obstruction, nasal bleeding and nasal borderline from 37 × 24 mm localize in the anterior part deformity. Biopsy have reveled moderaletly differenciated of right nasal cavity. This mass is enhanced heteroge- squamous cell carcinoma. After surgical procedure (lateral neous after contrast injection. A nasal bony destruction rhinotomy). The final diagnosis affirmed pleomorphic ade- is observed without lesion of adjacent structures (sinus- noma. es, orbit) (Figure 1 and Figure 2). Keywords Endonasal biopsy of tumor finds a moderately differ- Septal pleomorphic adenoma, Septal tumors, Immunohisto- entiated squamous cell carcinoma. pathology, Nasal septum The pre-therapeutic checkup is without anomalies. -
An Unusual Pleomorphic Adenoma
http://dx.doi.org/10.1590/1981-86372014000300000141930 CLÍNICO | CLINICAL An unusual pleomorphic adenoma Adenoma pleomórfico não usual Christiano Sampaio QUEIROZ1 Roberto Almeida de AZEVEDO1 Antonio Irineu TRINDADE NETO1 Caetano Guilherme Carvalho PONTES1 Rafael de Queiroz MOURA2 ABSTRACT Pleomorphic adenoma is the most common neoplasm in major and minor salivary glands. It constitutes approximately 90% of all benign salivary gland lesions and the parotid is the most affected location. When the minor salivary glands are affected, it mostly occurs at the junction of the hard and soft palates. The diagnosis is complex because of the great histological variety and biological behavior of this tumor, a histopathological examination being essential. The recommended treatment is surgical excision. For lesions located superficially in the parotid gland, superficial parotidectomy - identifying and preserving the facial nerve - is necessary. Lesions in the palate or gums sometimes demand a margin of safety, being excised below the periosteum, including the overlying mucosa. With correct surgical removal, the prognosis is excellent. The aim of this study is to report a case of an unusual minor salivary gland pleomorphic adenoma in the hard palate, describing the most important aspects of this pathology. Indexing terms: Neoplasms. Pleomorphic adenoma. Salivary glands. RESUMO O adenoma pleomórfico é a neoplasia mais comum entre os tumores das glândulas salivares maiores e menores. Constitui aproximadamente 90% de todas as lesões benignas das glândulas salivares e a parótida é a mais acometida. A junção dos palatos duro e mole é o sítio de predileção mais comum, quando as glândulas salivares menores são atingidas. O diagnóstico é complexo devido a grande variedade histológica e comportamento biológico deste tumor, sendo imprescindível a realização do estudo histopatológico. -
Lipomatous Pleomorphic Adenoma in the Palatine Gland
Oral Med Pathol 8 (2003) 139 Lipomatous Pleomorphic Adenoma in the Palatine Gland Kenichi Matsuzaka1, Hideki Fukumoto2, Chiaki Watanabe2, Masaki Shimono3 and Takashi Inoue1 1Oral Health Science Center and Dept. of Clinical Pathophysiology, Tokyo Dental College, Chiba, Japan 2Dept. of Oral Maxillofacial Surgery, National Mito Hospital, Ibaraki, Japan 3Oral Health Science Center and Dept. of Pathology, Tokyo Dental College, Chiba, Japan Matsuzaka K, Fukumoto H, Watanabe C, Shimono M and Inoue T. Lipomatous pleomorphic adenoma in the palatine gland. Oral Med Pathol 2003; 8: 139-140, ISSN 1342-0984 Lipomatous pleomorphic adenoma is an unusual subtype of adenoma with a lipomatous stromal component. Although there are a few reports about lipomatous pleomorphic adenoma in the parotid gland, we report an extremely rare case of lipomatous pleomorphic adenoma in the palatine gland of a 33-year-old female. Histologically, approximately 80% of the tumor tissue was fatty tissue containing univacuolar adipocytes. The pleomorphic epithelial elements consisted of duct-like cells forming small lumina and also consisted of spindle-shaped myoepithelial cells. Key words: lipomatous pleomorphic adenoma, palatine gland, adipocyte Correspondence: Kenichi Matsuzaka, Oral Health Science Center and Dept. of Clinical Pathophysiology, Tokyo Dental College, 1-2-2, Masago, Mihama-ku, Chiba 261-8502, Japan. Phone: +81-43-270-3581, Fax: +81-43-270-3583, E-mail: [email protected] Introduction Pathologically, the consistent histopathological feature Pleomorphic adenoma is the most common neo- was an encapsulated mass of epithelial and modified plasm of the salivary glands (1). Extensive lipomatous myoepithelial elements intermingled with duct-like struc- involvement of the stroma is a rare finding in pleomor- tures. -
Mesenchymal) Tissues E
Bull. Org. mond. San 11974,) 50, 101-110 Bull. Wid Hith Org.j VIII. Tumours of the soft (mesenchymal) tissues E. WEISS 1 This is a classification oftumours offibrous tissue, fat, muscle, blood and lymph vessels, and mast cells, irrespective of the region of the body in which they arise. Tumours offibrous tissue are divided into fibroma, fibrosarcoma (including " canine haemangiopericytoma "), other sarcomas, equine sarcoid, and various tumour-like lesions. The histological appearance of the tamours is described and illustrated with photographs. For the purpose of this classification " soft tis- autonomic nervous system, the paraganglionic struc- sues" are defined as including all nonepithelial tures, and the mesothelial and synovial tissues. extraskeletal tissues of the body with the exception of This classification was developed together with the haematopoietic and lymphoid tissues, the glia, that of the skin (Part VII, page 79), and in describing the neuroectodermal tissues of the peripheral and some of the tumours reference is made to the skin. HISTOLOGICAL CLASSIFICATION AND NOMENCLATURE OF TUMOURS OF THE SOFT (MESENCHYMAL) TISSUES I. TUMOURS OF FIBROUS TISSUE C. RHABDOMYOMA A. FIBROMA D. RHABDOMYOSARCOMA 1. Fibroma durum IV. TUMOURS OF BLOOD AND 2. Fibroma molle LYMPH VESSELS 3. Myxoma (myxofibroma) A. CAVERNOUS HAEMANGIOMA B. FIBROSARCOMA B. MALIGNANT HAEMANGIOENDOTHELIOMA (ANGIO- 1. Fibrosarcoma SARCOMA) 2. " Canine haemangiopericytoma" C. GLOMUS TUMOUR C. OTHER SARCOMAS D. LYMPHANGIOMA D. EQUINE SARCOID E. LYMPHANGIOSARCOMA (MALIGNANT LYMPH- E. TUMOUR-LIKE LESIONS ANGIOMA) 1. Cutaneous fibrous polyp F. TUMOUR-LIKE LESIONS 2. Keloid and hyperplastic scar V. MESENCHYMAL TUMOURS OF 3. Calcinosis circumscripta PERIPHERAL NERVES II. TUMOURS OF FAT TISSUE VI. -
The Role of Cytogenetics and Molecular Diagnostics in the Diagnosis of Soft-Tissue Tumors Julia a Bridge
Modern Pathology (2014) 27, S80–S97 S80 & 2014 USCAP, Inc All rights reserved 0893-3952/14 $32.00 The role of cytogenetics and molecular diagnostics in the diagnosis of soft-tissue tumors Julia A Bridge Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA Soft-tissue sarcomas are rare, comprising o1% of all cancer diagnoses. Yet the diversity of histological subtypes is impressive with 4100 benign and malignant soft-tissue tumor entities defined. Not infrequently, these neoplasms exhibit overlapping clinicopathologic features posing significant challenges in rendering a definitive diagnosis and optimal therapy. Advances in cytogenetic and molecular science have led to the discovery of genetic events in soft- tissue tumors that have not only enriched our understanding of the underlying biology of these neoplasms but have also proven to be powerful diagnostic adjuncts and/or indicators of molecular targeted therapy. In particular, many soft-tissue tumors are characterized by recurrent chromosomal rearrangements that produce specific gene fusions. For pathologists, identification of these fusions as well as other characteristic mutational alterations aids in precise subclassification. This review will address known recurrent or tumor-specific genetic events in soft-tissue tumors and discuss the molecular approaches commonly used in clinical practice to identify them. Emphasis is placed on the role of molecular pathology in the management of soft-tissue tumors. Familiarity with these genetic events -
Cutaneous Fetal Rhabdomyoma a Case Report and Historical Review of the Literature
CASE REPORT Cutaneous Fetal Rhabdomyoma A Case Report and Historical Review of the Literature Sarah N. Walsh, MD* and Mark A. Hurt, MDw mas; such articles have documented different histologic Abstract: Fetal rhabdomyomas are well-documented tumors, types, local regrowth and possible malignancy, a broader affecting both children and adults that are composed of age distribution, various immunohistochemical staining immature striated muscle at the sixth to tenth-week stage of patterns, occurrence in particular syndromes, and their development. Although there is often a predilection for the head presence in a wide assortment of organs and anatomic and neck region, these tumors have been identified in a wide sites.1,2,4–8,11,15,16,18,20–25,29,33 To the best of our knowl- array of anatomic sites. A primary cutaneous presentation, edge, however, fetal rhabdomyoma has never been however, has not yet been described. We report the first case of a diagnosed definitively in the skin. We present the first fetal rhabdomyoma arising in the skin of a 1-year old girl. After case of a cutaneous fetal rhabdomyoma found in a 1- the initial biopsy, an incomplete excision was performed with year-old girl with a lesion on the chin. tumor present histologically at multiple surgical margins. In a follow-up period of 54 months, there has been no lesional regrowth or evidence of further progression. This case is CASE REPORT detailed, in addition to a literature-based review of the historical The patient was a 1-year-old girl seen by a pediatric and conceptual development of the neoplasm known as fetal dermatologist for a chin lesion that had been present for the past 10 months but had not changed noticeably during that period. -
A Thesis Entitled
A Thesis entitled The Mechanisms of Malignant Transformation in Benign Salivary Gland Tumors Submitted by Yasmyne S. Castillo-Ronquillo MD As partial fulfillment of the requirements for the Master of Science in Biology _______________________________________ Adviser: Patricia Komuniecki Ph.D. _______________________________________ College of Graduate Studies The University of Toledo August 2009 An Abstract of The Mechanisms of Malignant Transformation in Benign Salivary Gland Tumors by Yasmyne S. Castillo-Ronquillo MD Submitted as partial fulfillment of the requirements for the Master of Science in Biology The University of Toledo August 2009 Tumors of the salivary glands are some of the most complex tumors known. Although the progression from a benign salivary gland tumor to a malignancy has been documented in the literature, this process is not well understood. Pleomorphic adenoma (PA) is a type of benign tumor known clinically and histopathologically to transform into a malignant form in both the salivary glands and lacrimal glands. Pleomorphic Adenoma Gene 1 (PLAG1) overexpression is the initial abnormality found in PA. The molecular changes in the progression from PA to early stages of malignancy have not been fully elucidated. However, the inactivation of tumor suppressor genes and the activation of oncogenes and proto-oncogenes appear to be involved in the early transition phase to malignancy. The inactivation of p53, the loss of DCC, p16 and the activation of the oncogenes p21, c-myc and c-ras have ii been documented in cell culture, animal studies and human salivary gland tumors. In the intermediate and late stage of the transformation of PA to a malignant carcinoma ex pleomorphic adenoma (CXPA), the cell cycle genes CDC25A, erb-2, cdk-4, E2F- 1, Bub-1, STAT3 are involved. -
Pleomorphic Adenoma a Salivary Gland Tumor As Nasal Mass; Rarest Presentation
Global Journal of Otolaryngology ISSN 2474-7556 Case Report Glob J Otolaryngol - Volume 3 Issue 3 January 2017 Copyright © All rights are reserved by Bhushan Kathuria DOI: 10.19080/GJO.2017.03.555613 Pleomorphic Adenoma a Salivary Gland Tumor as Nasal Mass; Rarest Presentation *Bhushan Kathuria1, Dinesh Madhur2, Himani Dhingra3 and Mohit Pareek4 1Consultant, Department of Otolaryngology, Head & Neck Surgery, Aadhar Hosital, India 2Senior resident, Department of Otolaryngology, Head & Neck Surgery, Agroha medical college, India 3Senior resident, Department of paediatric, Sion hospital Mumbai, India 4Resident, Department of Otolaryngology, Head & Neck Surgery, Post Graduate Institute of Medical Sciences, India Submission: December 27, 2016; Published: January 23, 2017 *Corresponding author: Bhushan Kathuria, Consultant, Department of Otolaryngology, Head & Neck Surgery, Aadhar Hosital, Hissar, Haryana, India, Email: Abstract Pleomorphic adenoma of minor salivary glands can be seen at any location where minor salivary glands are present such as neck, ear, external nose and nasal cavity. However the lesions detected in nasal cavity are extremely rare. Here we describing a case of intranasal pleomorphic adenoma of the nasal septum who was previously treated as chronic sinusitis but after further investigation the correct diagnosis was made and treated accordingly. Keywords: Nasal Mass; Pleomorphic Adenoma; Endoscopic Resection Introduction rigid endoscopy of the nose showed that the polypoidal mass Salivary gland tumors represent 3% of all head and neck seemed to originate from the nasal septum and protruding into tumors. Among these 85-90% originates from the major salivary right nasal cavity with mucopurulent discharge, touching lateral glands. Pleomorphic adenoma is the most common benign nasal wall at level of the middle turbinate and blocking right side salivary gland tumor. -
346 Fetal Cardiac Rhabdomyoma: a Case Report
A CASE REPORT Bali Medical Journal (Bali Med J) 2016, Volume 5, Number 3: 543-546 P-ISSN.2089-1180, E-ISSN.2302-2914 Fetal cardiac rhabdomyoma: a case report A Case Report Tjokorda Gde Agung Suwardewa,1* I Ketut Surya Negara,1 AAN Jaya Kusuma,1 AAP Wiradnyana,1 Ryan Mulyana Surya,1 I Ketut Tunas2 CrossMark Doi: http://dx.doi.org/10.15562/bmj.v5i3.346 Published by DiscoverSys ABSTRACT Volume No.: 5 Background: Fetal cardiac rhabdomyoma is a rare condition. tomography scan, to rule out anything related to tuberous sclerosis. Case: We report a case with cardiac mass discovered in utero by The prognosis depends on the size, site, number of tumors, and co- prenatal ultrasonography at 33 weeks of gestational age. An echogenic existing congenital abnormalities. Management highly depends on Issue: 3 round-oval shape mass at the interventricular septum protrudes to left the presence of outflow tract obstruction of the heart. However, some ventricle was observed. cases may regress after birth. Results: After birth, the baby was followed up for 7 months with echocardiography, physical examination, and computerized First page No.: 543 Keywords: rhabdomyoma, fetal heart, tuberous sclerosis. Cite This Article: Suwardewa, T., Surya Negara, I., Jaya Kusuma, A., Wiradnyana, A., Surya, R., Tunas, I. 2016. Fetal cardiac rhabdomyoma: a case P-ISSN.2089-1180 report. Bali Medical Journal 5(3): 543-546. DOI:10.15562/bmj.v5i3.346 1Department of Obstetrics and INTRODUCTION rhabdomyoma, which found incidentally during a E-ISSN.2302-2914 Gynecology, Udayana University / routine antenatal visit. Sanglah Hospital Denpasar, Bali- The presence of a primary congenital tumor of Indonesia.