scholarly journals Superficial Acral Fibromyxoma. Un Uncommon Tumor of the Foot

2019 ◽  
Vol 13 (4) ◽  
pp. 251-4
Author(s):  
Santiago Pache ◽  
Rodrigo Fratelli ◽  
Javier Cedrani ◽  
Paola Filomeno ◽  
Thomas Clanton
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Female Patient ◽  
Soft Tissue Tumor ◽  
Wide Resection ◽  
Level Of Evidence ◽  
Fifth Toe ◽  
Hands And Feet ◽  
Superficial Acral Fibromyxoma ◽  
Uncommon Tumor

This study presents a case report of a 52-year-old female patient with a superficial acral fibromyxoma (SAF) of her left foot fifth toe. This is a very uncommon soft tissue tumor that affects mainly hands and feet, with a special predilection for toes, with the hallux most frequent. The tumor in this case was 3cm long and 2.5cm wide, which was unusually large. Few cases are larger than 2cm long and localized on the fifth toe. Thetreatment was wide resection of the tumor through amputation of the fifth toe. Level of Evidence V; Therapeutic Studies; Expert Opinion.

scholarly journals Management of a soft tissue tumor in a child with Worster Drought syndrome using 810 nm diode laser - A case report

LASER THERAPY ◽  
2015 ◽  
Vol 24 (2) ◽  
pp. 113-117
Author(s):  
Praveen Kumar Jayakumar ◽  
Jayakumar Paramasivam ◽  
Naveen Kumar Jayakumar ◽  
Gayathri Praveen Kumar ◽  
Alex Mathews Muruppel
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Diode Laser ◽  
Soft Tissue Tumor ◽  
Tissue Tumor

scholarly journals GIST of Mesocolon: A Case Report

2012 ◽  
Vol 10 (1) ◽  
pp. 37-39
Author(s):  
S Malla ◽  
SB Rawal ◽  
NK Giri
Keyword(s):  
Medical Journal ◽  
Case Report ◽  
Clinical Practice ◽  
Soft Tissue ◽  
Gastrointestinal Stromal Tumor ◽  
World Literature ◽  
Rare Case ◽  
Soft Tissue Tumor ◽  
Tissue Tumor ◽  
The World

Gastrointestinal Stromal Tumor (GIST) is a rare soft tissue tumor and a GIST arising from the mesocolon is even rarer and sparsely reported in the world literature. Herein we report one such case that we encountered in our clinical practice and review the literature on the management of such a rare case. DOI: http://dx.doi.org/10.3126/mjsbh.v10i1.6448 Medical Journal of Shree Birendra Hospital Jan-June 2011 10(1) 37-39

scholarly journals IgG4-Related Disease Presenting as a Soft Tissue Tumor Affecting Skeletal Muscle: A Case Report

2013 ◽  
Vol 04 (12) ◽  
pp. 1-4 ◽  
Author(s):  
David Sáez Martínez ◽  
Felipe López Oliva ◽  
María Jesús Fernández Aceñero ◽  
Elena Fontoira Moyer ◽  
Juan Luis Arranz Cozar
Keyword(s):  
Skeletal Muscle ◽  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Related Disease ◽  
Tissue Tumor ◽  
Igg4 Related Disease

scholarly journals CLINICOPATHOLOGIC, DERMOSCOPIC AND ULTRASOUND EXAMINATION OF A RARE ACRAL TUMOUR INVOLVING THE NAIL- A CASE REPORT AND REVIEW OF THE LITERATURE

2016 ◽  
Vol 89 (1) ◽  
pp. 160-164 ◽  
Author(s):  
Lavinia Elena Grigore ◽  
Corina Iulia Baican ◽  
Carolina Botar-Jid ◽  
Liliana Rogojan ◽  
Alina Florentina Letca ◽  
...  
Keyword(s):  
Case Report ◽  
Preoperative Assessment ◽  
Short Review ◽  
Wide Resection ◽  
Resection Margins ◽  
Review Of The Literature ◽  
Non Invasive ◽  
First Case ◽  
Nodular Lesions ◽  
Superficial Acral Fibromyxoma

There is a large spectrum of tumors presenting as nodular lesions that may affect the subungual space. We report the case of a 62-year-old woman presenting with a rapidly growing nodular lesion under the nail of the first left toe. Non-invasive examinations using dermoscopy, ultrasonography and elastography were performed for the preoperative assessment of the lesion. The biopsy of the lesion revealed superficial acral fibromyxoma, a benign tumor with predisposition for acral sites. The patient underwent radical surgery with wide resection margins. This is the first case report of a superficial acral fibromyxoma affecting the subungual region characterized by dermoscopic, ultrasonographic and elastographic features. We also performed a short review of the literature.

scholarly journals Lipomas of Larynx: The Rare Entities

2012 ◽  
Vol 2 (2) ◽  
pp. 79-81 ◽  
Author(s):  
Somanath B Megalamani ◽  
Ravindra Gadag ◽  
A Raza ◽  
A Satish
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Tumor ◽  
Spindle Cell ◽  
Anterior Commissure ◽  
The Body ◽  
Spindle Cell Lipoma ◽  
Tissue Tumor

ABSTRACT Lipoma is the commonest soft tissue tumor arising anywhere in the body, but its occurrence in the larynx is relatively rare. We present a rarest case of lipoma with cartilaginous metaplasia arising from the larynx just above the anterior commissure. The second case report is about a large spindle cell lipoma of larynx presented with stridor. How to cite this article Megalamani SB, Gadag R, Raza A, Satish A. Lipomas of Larynx: The Rare Entities. Int J Phonosurg Laryngol 2012;2(2):79-81.

scholarly journals A CASE REPORT OF FEMUR OSTEOCHONDROMA IN 22 YEARS OLD FEMALE PATIENT

2020 ◽  
Vol 8 (10) ◽  
pp. 1263-1267
Author(s):  
Abdulrahman M. Bin Mohi ◽  
◽  
Ahmed A. Alzahrani ◽  
Bashar R. Reda
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Proximal Femur ◽  
Conflict Of Interest ◽  
Distal Femur ◽  
Tumor Resection ◽  
Surgical Excision ◽  
Low Grade ◽  
The Right ◽  
Hands And Feet

Chondromais considered a nonmalignant tumor that composed of mature hyaline cartilage and commonly occur in hands and feet. Overall incidents show that females are predominant comparing to males with evenly distributed range of ages. Multiple chondromas have to be differentiated from osteochondroma and chondrosarcoma. This paper reports three different types of lesions in one patient.Osteochondroma or exostosis is the most common benign tumor of the skeleton. It is a developmental osseous anomaly, which arises from exophytic outgrowth on bone surfaces characteristically. Osteochondroma account for about 12% of bone tumors. Here, we have described a 22 years old female patient with left knee joint pain and swelling of the left distal femur with limited movements. The incisional biopsy of the left distal femur identified low-grade chondrosarcoma and chondroma after histopathology. This underwent one-stage surgical excision of the tumor with a posterior approach and tumor resection from the femur. After surgery, an unusual pain appears in the right hip joint during the post-operative period.Machine resonance imaging (MRI), and X-ray of pelvis help to diagnose thewell-differentiated chondrosarcoma and chondroma. This was a case of osteochondroma in the right proximal femur, chondroma like lesion in the left proximal femur and chondrosarcoma in the left distal femur. Ethical consideration: Written informed consent was obtained from the patient for publication of this case report and accompanying images. Conflict of interest: There is no conflict of interest.

scholarly journals A Case Report of a Giant Adrenal Angiomyolipoma at Computed Tomography

2020 ◽  
Vol 2 (1) ◽  
pp. 42-43
Author(s):  
Francesco Messina ◽  
Lorena Turano ◽  
Nicola Arcadi
Keyword(s):  
Computed Tomography ◽  
Abdominal Pain ◽  
Case Report ◽  
Adrenal Gland ◽  
Female Patient ◽  
Uncommon Tumor

Angiomyolipoma of the adrenal gland is an extremely uncommon tumor detected incidentally in studies for other pathologies. We present the case of a 55-year-old female patient with a giant incidental right adrenal angiomyolipoma, detected by Computed Tomography (CT), performed for abdominal pain.

Sign in / Sign up

Export Citation Format

Share Document