Multiple Eccrine Syringofibroadenoma of Mascaro of the Lower Extremity

2016 ◽  
Vol 106 (6) ◽  
pp. 433-438
Author(s):  
Danae L. Lowell ◽  
Nichol L. Salvo ◽  
William J. Weily ◽  
Michael Swiatek ◽  
Hannah Sahli
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lower Extremity ◽  
Benign Lesion ◽  
Unknown Etiology ◽  
Secretory Differentiation

Eccrine syringofibroadenoma (ESFA) is a rare benign lesion of ductal and secretory differentiation exhibiting multiple cutaneous polymorphic presentations with an unknown etiology. We present a case of ESFA that uniquely exhibited large, thick, verrucous-like hyperplastic growths as well as superficial shiny mosaic plaques and deep ulcerations in three different anatomical locations in the same patient. The diagnosis of ESFA was confirmed histologically after biopsies were performed on all of the affected areas. In addition to a case report and literature review, we also present classification, clinical, and histologic aspects of ESFA.

Adenoid Cystic Carcinoma on Tongue Misdiagnosed as Benign Lesion: A Case Report and Literature Review

2021 ◽  
Vol 45 (4) ◽  
pp. 127-132
Author(s):  
Yoon-Hee Ma ◽  
◽  
Changmo Sohn ◽  
Mi-Heon Ryu ◽  
Dae-Seok Hwang
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Adenoid Cystic Carcinoma ◽  
Benign Lesion ◽  
Adenoid Cystic

scholarly journals Geographic Stomatitis with Multiple Areas Involvement of Oral Cavity: A Case Report and Review of Literatures

2021 ◽  
Vol 10 ◽  
pp. 2107
Author(s):  
Farid Abbasi ◽  
Aliyeh Sehatpour ◽  
Seyed Masoud Sajedi ◽  
Parisa Bahadori ◽  
Mohadeseh Nouri
Keyword(s):  
Case Report ◽  
Oral Cavity ◽  
Oral Mucosa ◽  
Benign Lesion ◽  
Ventral Surface ◽  
Unknown Etiology ◽  
Clinical Appearance ◽  
Clinicopathologic Findings ◽  
Characteristic Features ◽  
Rule Out

Background: Geographic stomatitis is an uncommon migratory benign lesion of oral mucosa with unknown etiology. It can affect all the areas of the oral mucosa, but the dorsum and lateral borders of the tongue are the most commonly involved areas called geographic tongue. The clinical appearance of this condition is the oval or circular erythematous areas with irregular elevated keratotic borders. These characteristic features of geographic stomatitis are diagnostic for all clinicians when appearing on the dorsum of the tongue, despite other affected areas of oral mucosa that can confuse clinicians. This condition may be associated with some diseases such as psoriasis, Reiter’s syndrome, and atopic conditions, so the clinicians should rule out these diseases and diagnose the geographic stomatitis. Case Report: A 17-year-old male attended to our department for a routine dentistry checkup. During the intraoral examination, we found multiple erythematous areas surrounded by a thin white border on different surfaces of his oral cavity. His extraoral examinations were completely normal. Conclusion: Due to the rarity of this lesion on the other sites of oral mucosa rather than dorsum and lateral borders of the tongue such as labial mucosa, buccal mucosa, the floor of the mouth, ventral surface of the tongue, and palate, it is necessary to report, study and evaluate each case of this condition that clinicopathologic findings have confirmed this diagnosis, to treat and advice these patients on the best approach. [GMJ.2021;10:e2071]

scholarly journals Keratosis Lichenoides Chronica – a Case Report and Literature Review

2014 ◽  
Vol 6 (3) ◽  
pp. 120-137
Author(s):  
Mirjana Paravina ◽  
Predrag Cvetanović ◽  
Miloš Kostov ◽  
Slađana Živković ◽  
Ivana Dimovski ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Rare Disease ◽  
Clinical Picture ◽  
Treatment Options ◽  
Clinical Manifestations ◽  
Poor Response ◽  
Unknown Etiology ◽  
Distinct Entity

Abstract Keratosis lichenoides chronica represents a distinct entity, a rare disease of unknown etiology and pathogenesis, with clinical manifestations which, although typical, require extensive differential diagnosis. The course of the disease is chronic, progressive, and it is resistant to various treatment options, so despite variations in the clinical picture it is really easier to diagnose than to treat. This is a case report of a male patient in whom the diagnosis of keratosis lichenoides chronica was based on typical clinical picture, repeated biopsies and histopathological findings, course of the disease and poor response to any therapy.

scholarly journals HISTOCYTOPATHOLOGICAL DIAGNOSIS OF ROSAI-DORFMAN DISEASE: CASE REPORT AND LITERATURE REVIEW

2021 ◽  
Author(s):  
Zephania Abraham ◽  
Zerd Francis ◽  
Advera Ngaiza ◽  
Aveline Kahinga ◽  
Faustine Bukanu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Sinus Histiocytosis ◽  
Unknown Etiology ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Disease Case

Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self-limiting disease of the cells of macrophage-histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massive bilateral cervical and submandibular lymphadenopathy, diagnosed by histocytopathology.

scholarly journals Plasma Cell Gingivitis as a Predisposing Factor for Plaque-Induced Periodontitis: A Case Report

2021 ◽  
pp. 71-74
Author(s):  
Vilma Alejandra Umanzor Bonilla ◽  
Claudette Arambú ◽  
Hugo Romero ◽  
Juan Jose Guifarro
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Plasma Cell ◽  
Plasma Cells ◽  
Benign Lesion ◽  
Unknown Etiology ◽  
Histopathological Study ◽  
Predisposing Factor ◽  
Gingival Bleeding ◽  
Gingival Enlargement

Plasma cell gingivitis is a benign lesion of unknown etiology characterized by massive infiltration of plasma cells into the connective tissue of the gingiva. Clinically it presents as a gingival enlargement with erythema and some areas with the presence of desquamation, it is usually asymptomatic, but on some occasions the patient may present pain and gingival bleeding. Diagnosis requires clinical-pathological correlation. Based on the foregoing, we present a case report of a 25-year-old female patient diagnosed with plasma cell gingivitis with idiopathic etiology based on the clinical and histopathological study.

scholarly journals Tongue Osseous Choristoma in an 11-Year-Old Female: A Case Report and Literature Review Focusing on Pediatric Cases

2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
Satomi Arimoto ◽  
Manabu Shigeoka ◽  
Masaya Akashi
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Literature Review ◽  
Pediatric Patient ◽  
Benign Lesion ◽  
Excisional Biopsy ◽  
Clinicopathological Characteristics ◽  
Dental Clinic ◽  
Postoperative Course ◽  
Mature Bone

Osseous choristoma is an uncommon benign lesion characterized by the presence of ectopic mature bone within soft tissue. In most cases, these lesions occur on the dorsum of the tongue in patients in their third and fourth decades of life. This article describes a case of lingual osseous choristoma in a pediatric patient. An eleven-year-old girl with a lingual mass was referred to our hospital from a dental clinic. Total excisional biopsy and histological examination were performed, and osseous choristoma was diagnosed. The postoperative course was uneventful with no signs of recurrence during the 12 months after surgery. Moreover, a literature review focusing on pediatric cases with lingual osseous choristoma was performed to know the etiology, clinicopathological characteristics, and course of treatment of the lesion.

Cutaneous angiosarcoma. A literature review and case report

1990 ◽  
Vol 80 (9) ◽  
pp. 501-504 ◽  
Author(s):  
K Wolf ◽  
J Pasquino
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Literature Review ◽  
Lower Extremity ◽  
Soft Tissue Tumor ◽  
Surgical Excision ◽  
Tissue Tumor ◽  
Pigmented Lesion ◽  
Malignant Soft Tissue Tumor ◽  
Malignant Soft Tissue

A case of angiosarcoma of the lower extremity was presented. This rare but highly malignant soft tissue tumor usually presents as a raised pigmented lesion. Wide surgical excision or amputation is the treatment of choice. Radiotherapy may offer some relief in cases that are inoperable.

Spontaneous Spinal Epidural Hematoma of Unknown Etiology: Case Report and Literature Review

2008 ◽  
Vol 9 (2) ◽  
pp. 242-246 ◽  
Author(s):  
Robert H. Thiele ◽  
Ziad A. Hage ◽  
Daniel L. Surdell ◽  
Stephen L. Ondra ◽  
H. Hunt Batjer ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Epidural Hematoma ◽  
Spinal Epidural Hematoma ◽  
Unknown Etiology ◽  
Spontaneous Spinal Epidural Hematoma ◽  
Spinal Epidural
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