Red, Exophytic Nodule of the Plantar Foot

2015 ◽  
Vol 105 (2) ◽  
pp. 195-197 ◽  
Author(s):  
Mary-Margaret Kober ◽  
Usha Alapati ◽  
Amor Khachemoune
Keyword(s):  
Elderly Patient ◽  
Differential Diagnosis ◽  
Pyogenic Granuloma ◽  
Amelanotic Melanoma ◽  
Vascular Tumors ◽  
Diagnostic Challenge ◽  
Biopsy Technique ◽  
Plantar Surface ◽  
Foot Lesions ◽  
Eccrine Poroma

Pyogenic granulomas are benign vascular tumors characterized histologically by a lobular proliferation of capillaries. We report an unusual presentation of a pyogenic granuloma in an elderly patient with a bleeding red nodule on the plantar surface of the foot. Nodular exophytic plantar foot lesions often present a diagnostic challenge, as the differential diagnosis includes benign and malignant entities ranging from eccrine poroma and pyogenic granuloma to Kaposi's sarcoma and amelanotic melanoma. This case highlights the need for an adequate biopsy technique to confirm the diagnosis and guide management.

scholarly journals Amelanotic melanoma and pyogenic granuloma. Peculiarities of the differential diagnosis

2020 ◽  
Vol 23 (4) ◽  
pp. 202-207
Author(s):  
Azizzhon D. Zikiryachodzhaev ◽  
E. K. Saribekyan ◽  
E. Yu. Vertieva ◽  
I. S. Pestin
Keyword(s):  
Differential Diagnosis ◽  
High Risk ◽  
Pyogenic Granuloma ◽  
Amelanotic Melanoma ◽  
Invasive Procedures ◽  
Skin Tumour ◽  
Non Invasive ◽  
Early Stages ◽  
Vascular Formation

INTRODUCTION:Nodular melanoma is a rapidly progressive skin tumour with a high risk of methastasis even on early stages. This fact leads to necessity of non-invasive procedures, which can verify this diagnosis before surgery. Nodular forms of amelanotic melanoma can be hardly diagnosed because of their unusual diagnostic and dermatoscopic features. CASE REPORT:Pyogenic granuloma is the most difficult disease for differential diagnosis. It is a benign vascular formation, which mimics nodular amelanotic melanoma.

Eccrine Poroma: A Differential Diagnosis in Chronic Foot Lesions

2003 ◽  
Vol 24 (10) ◽  
pp. 789-792 ◽  
Author(s):  
Margaret W. N. Wong ◽  
Gary M. K. Tse
Keyword(s):  
Differential Diagnosis ◽  
Foot Lesions ◽  
Eccrine Poroma

Rectovaginal extragastrointestinal stromal tumour (EGIST): an additional entity to be considered in the differential diagnosis of tumours of the rectovaginal septum

2021 ◽  
Vol 14 (3) ◽  
pp. e237669
Author(s):  
Susan Addley ◽  
Moiad Alazzam ◽  
Catherine Johnson ◽  
Hooman Soleymani majd
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
High Risk ◽  
Kinase Inhibitor ◽  
Correct Diagnosis ◽  
Rectovaginal Septum ◽  
Gastrointestinal Stromal Tumours ◽  
Diagnostic Challenge ◽  
High Quality ◽  
Primary Surgery

Gastrointestinal stromal tumours (GISTs) are rare - and rectovaginal extragastrointestinal stromal tumours (RV-EGISTs) even rarer. We share a case of RV-EGIST, complemented by high-quality radiological and surgical images. A review of current literature pertaining to RV-EGIST is also included. Our case report highlights the diagnostic challenge presented by extragastrointestinal stromal tumours. Differentiated from overlapping pathologies only by targeted application of immunohistopathology and cytogenetics, the inclusion of RV-EGIST in the differential diagnosis of a rectovaginal tumour is essential to making this correct diagnosis. Primary surgery is the treatment of choice for RV-EGIST if complete cytoreduction can be achieved, combined with adjuvant tyrosine kinase inhibitor (TKI) therapy for those with high-risk features to further reduce rates of future recurrence.

scholarly journals Pyogenic granuloma of tongue: A rare case report

2014 ◽  
Vol 6 (3) ◽  
pp. 84-86
Author(s):  
Sonam Sharma ◽  
Amita Sharma ◽  
Ashok Kumar ◽  
Shivani Kalhan ◽  
Jasmine Kaur
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Male Patient ◽  
Rare Case ◽  
Pyogenic Granuloma ◽  
Definitive Diagnosis ◽  
Medical Sciences ◽  
New Approaches ◽  
Rare Case Report ◽  
Chronic Irritation

Pyogenic granuloma (PG) is a kind of inflammatory hyperplasia in response to chronic irritation. Here, we report a case of 64 year old male patient with PG on midline of the dorsum of the posterior third of the tongue. Its differential diagnosis, the importance of biopsy findings in establishing definitive diagnosis and about the new approaches for its treatment is discussed. DOI: http://dx.doi.org/10.3126/ajms.v6i3.10619Asian Journal of Medical Sciences Vol.6(3) 2015 84-86

scholarly journals Cardiac Outpouchings: Definitions, Differential Diagnosis, and Therapeutic Approach

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Riccardo Scagliola ◽  
Gian Marco Rosa ◽  
Sara Seitun
Keyword(s):  
Differential Diagnosis ◽  
Clinical Practice ◽  
Therapeutic Approach ◽  
Tissue Characterization ◽  
Case Reports ◽  
Case Series ◽  
Diagnostic Challenge ◽  
Comprehensive Overview ◽  
Search Data ◽  
Data Location

Background and Aims. Cardiac outpouchings encounter a series of distinct congenital or acquired entities (i.e. aneurysms, pseudoaneurysms, diverticula, and herniations), whose knowledge is still poorly widespread in clinical practice. This review aims to provide a comprehensive overview focusing on definition, differential diagnosis, and prognostic outcomes of cardiac outpouchings, as well as further insights on therapeutic options, in order to assist physicians in the most appropriate decision-making. Methods. The material reviewed was obtained by the following search engines: MEDLINE (PubMed), EMBASE, Google Scholar, and Clinical Trials databases, from January 1966 until March 2021. We searched for the following keywords (in title and/or abstract): (“cardiac” OR “heart”) AND (“outpouching” OR “outpouch” OR “aneurysm” OR “pseudoaneurysm” OR “false aneurysm” OR “diverticulum” OR “herniation”). Review articles, original articles, case series, and case reports with literature review were included in our search. Data from patients with congenital or acquired cardiac outpouchings, from prenatal to geriatric age range, were investigated. Results. Out of the 378 papers initially retrieved, 165 duplicates and 84 records in languages other than English were removed. Among the 129 remaining articles, 76 were included in our research material, on the basis of the following inclusion criteria: (a) papers pertaining to the research topic; (b) peer-reviewed articles; (c) using standardized diagnostic criteria; and (d) reporting raw prevalence data. Location, morphologic features, wall motion abnormalities, and tissue characterization were found to have a significant impact in recognition and differential diagnosis of cardiac outpouchings as well as to play a significant role in defining their natural history and prognostic outcomes. Conclusions. Careful recognition of cardiac outpouchings remains a diagnostic challenge in clinical practice. Due to a broad cluster of distinctive and heterogeneous entities, their knowledge and timely recognition play a pivotal role in order to provide the most appropriate clinical management and therapeutic approach.

A Case of Auricular Pseudocyst

2016 ◽  
Vol 20 (6) ◽  
pp. 573-574 ◽  
Author(s):  
Vanessa Cohen ◽  
Geneviève Fortier-Riberdy ◽  
Issam Saliba ◽  
Sandra Davar
Keyword(s):  
Differential Diagnosis ◽  
Diagnosis And Treatment ◽  
Treatment Modalities ◽  
Diagnostic Challenge

Background: Auricular pseudocyst is a rare, asymptomatic, cystic-like swelling of the auricle that may pose a diagnostic challenge to the clinician. If inadequately treated, recurrences and ear deformities may ensue. Objective: The authors present a case of auricular pseudocyst in a previously healthy 43-year-old man. Aetiologies, histology, differential diagnosis, and treatment modalities are discussed.

Pyogenic Granuloma of the Foot with Satellitosis: A Role for Conservative Management

2011 ◽  
Vol 15 (1) ◽  
pp. 58-60
Author(s):  
Janice Bacher ◽  
Dalal Assaad ◽  
David N. Adam
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Conservative Management ◽  
Treatment Options ◽  
Pyogenic Granuloma ◽  
Conservative Approach ◽  
Review Of The Literature ◽  
Atypical Case ◽  
Over Time ◽  
Rule Out

Background: Pyogenic granuloma (PG) with satellitosis is a rare phenomenon that typically occurs in children and teenagers. It can be seen after excision or trauma to the original lesion. Objective: The aim is to review an atypical case of PG with satellitosis and to highlight a conservative approach to management. Methods: This article includes a case report of a 48-year-old woman developing PG with satellitosis in her right foot and includes a review of the literature. Results: There are few cases of PG with satellitosis in the literature. Our patient differs from most given her age and the location of the lesions. She was managed differently with a conservative observational approach, and, over time, her symptoms abated. Conclusion: PG with satellitosis can occur in varying patient populations with varying presentations. Although several treatment options exist, managing patients conservatively should be considered an approach to management. Early investigations should be conducted to rule out more sinister items in the differential diagnosis.

Solitary neurofibroma of the larynx: a diagnostic challenge

2021 ◽  
Vol 14 (1) ◽  
pp. e236682
Author(s):  
Bruno Cunha ◽  
Ricardo Pacheco ◽  
Isabel Fonseca ◽  
Alexandra Borges
Keyword(s):  
Differential Diagnosis ◽  
Tumour Size ◽  
Negative Consequences ◽  
Diagnostic Challenge ◽  
Presenting Symptoms ◽  
Aged Woman ◽  
Complete Surgical Resection ◽  
Long Term Follow Up ◽  
Middle Aged Woman ◽  
Benign Nature

Solitary neurofibromas of the larynx are extremely rare, with a total of 15 cases described in the literature. Nonetheless, acquaintance with this diagnosis is important, as misdiagnoses can have negative consequences. Presenting symptoms are non-specific and depend on tumour size and location. As well-defined submucosal masses with a broad differential diagnosis, they remain a clinical and radiological challenge. While some characteristics might favour a benign nature and subtle signs might help narrow the differential diagnosis, imaging alone is not sufficient for differentiation and definitive diagnosis requires a biopsy. Complete surgical resection and long-term follow-up is indicated. We share our experience on a case of a solitary laryngeal neurofibroma in a middle-aged woman, presenting with a large well-defined paraglottic lesion.

Malignant Deciduoid Mesothelioma: A Diagnostic Challenge

2005 ◽  
Vol 129 (3) ◽  
pp. 403-406 ◽  
Author(s):  
Najat Mourra ◽  
Cecilede Chaisemartin ◽  
Isabelle Goubin-Versini ◽  
Rolland Parc ◽  
Jean-Francois Flejou
Keyword(s):  
Differential Diagnosis ◽  
Cesarean Section ◽  
Tumor Cells ◽  
Elderly People ◽  
Young Women ◽  
Poor Prognosis ◽  
Diagnostic Challenge ◽  
Keratin 5 ◽  
The Poor ◽  
Rare Phenotype

Abstract Malignant deciduoid mesothelioma, a rare phenotype of epithelioid mesothelioma, arises more commonly from the peritoneum of young women, but it is also reported in the pleura of elderly people. We report a case of malignant deciduoid mesothelioma that occurred in a 41-year-old woman after cesarean section and was initially misdiagnosed as pseudotumoral deciduosis. Microscopically, the tumor was entirely composed of deciduoid areas, and only scattered tumor cells were positive for calretinin and keratin 5/6. The patient died 14 months after the first operation. This observation confirms the poor prognosis of this entity and the importance of the differential diagnosis of pseudotumoral deciduosis.

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