scholarly journals Nasolabial hamartoma: a rare case report

2020 ◽  
Vol 6 (7) ◽  
pp. 1397
Author(s):  
D. Senthamarai Kannan ◽  
G. Soundara Rajan ◽  
Veerasigamani Narendrakumar ◽  
V. K. Sathiya
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Surgical Excision ◽  
The Body ◽  
Nasolabial Fold ◽  
Tissue Development ◽  
Inborn Errors ◽  
Complete Surgical Excision ◽  
Rare Case Report

<p class="abstract">Nasolabial cysts are rare, nonodontogenic soft tissue developmental cysts occur in the maxillary lip and nasal alar regions. Patients usually presents with an asymptomatic soft swelling with obliteration of the nasolabial fold. Due to it's origin from entrapped epithelium in an embryonic fusion plane developmentally, this cyst is considered to be a Hamartoma. Hamartomas are non-neoplastic malformations, or inborn errors of tissue development. They are characterized by an abnormal mixture of tissues indigenous to that area of the body. Complete surgical excision is the accepted method of treatment. This report aimed to present a case of nasolabial cyst hamartoma, which is rare in presentation.</p>

scholarly journals A maxillary ameloblastic fibrosarcoma tumor: a rare case report from Syria

2020 ◽  
Vol 2020 (8) ◽  
Author(s):  
Amjad Soltany ◽  
Ghazal Asaad ◽  
Rami Daher ◽  
Mouhannad Dayoub ◽  
Ali Khalil ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Soft Tissue Sarcomas ◽  
Surgical Excision ◽  
Low Grade ◽  
Rare Case Report ◽  
Ameloblastic Fibrosarcoma ◽  
The Right

Abstract Ameloblastic fibrosarcoma (AFS) is a rare, aggressive malignant odontogenic tumor. AFS is seen most frequently in second and third decades of life. We are reporting a case of a low grade AFS in a 21-year-old male complaining of a painless swelling in the right side of the maxilla. The patient was treated with surgical excision followed by radiotherapy, which is considered the most effective approach for most of soft tissue sarcomas. AFS has a high-reported recurrence rate (up to 37%); therefore, long-term surveillance for recurrence is crucial.

scholarly journals Epiglottic dermoid cyst: a rare case report

2021 ◽  
Vol 7 (8) ◽  
pp. 1381
Author(s):  
Ramchandra . ◽  
C. B. Nandyal ◽  
Kiran Deshmukh
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Rare Case ◽  
English Literature ◽  
Age Groups ◽  
Neck Region ◽  
Surgical Excision ◽  
Complete Surgical Excision ◽  
Body Sensation ◽  
Rare Case Report

<p>Epiglottis dermoid cysts are generally benign lesions, which can affect all the age groups. Dermoid cysts arising from the head and neck region are rare, slow growing, and well-circumscribed neoplasm. Symptoms are non-specific and usually related to the size and the location of the lesion. A dermoid cyst of the epiglottis is extremely rare. To the best of our knowledge, only one case has been previously reported in the English literature and a total of three cases were presented in Russian literature in two studies. In our report, a middle-aged male presented with foreign body sensation in throat for 1-year and difficulty in swallowing for three months, mainly for solids. Thorough history, clinical examination and relevant investigation were done. Direct laryngoscopy was done and complete surgical excision was done. The aim of the case report is to present a rare case of epiglottic dermoid cyst, its clinical presentation, radio-logical features and surgical management.</p>

scholarly journals Primary Cutaneous Actinomycosis of Lower Extremity: A Rare Case Report

2015 ◽  
Vol 6 (1) ◽  
pp. 55-57
Author(s):  
Mohammad Ismail Hossain ◽  
AKM Shahabuddin Khan
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Lower Extremity ◽  
Rare Case ◽  
Extended Period ◽  
Surgical Excision ◽  
Lateral Aspect ◽  
Medical College ◽  
Rare Case Report ◽  
Direct Inoculation

Actinomycosis is a chronic, suppurative, and granulomatous process caused by actinomycetes, saprophytic bacteria normally residing in the oral cavity. There are a few cases of primary actinomycosis described in the literature where it can involve any organ. Primary cutaneous actinomycosis of the lower extremity is very uncommon and can easily be regarded as ordinary soft tissue infection. Herein, a case of 45-year-old diabetic man with primary cutaneous actinomycosis at his lower extremity, over the lateral aspect of left lateral maleolus, probably after direct inoculation of the microorganism from his saliva into a preceding wound in extremity, was reported. He was treated successfully with surgical excision combined with extended period of antimicrobial treatment.Anwer Khan Modern Medical College Journal Vol. 6, No. 1: January 2015, Pages 55-57

scholarly journals Anesthetic Management of a Large Retroperitoneal Paraganglioma: A Rare Case Report

2020 ◽  
pp. 1-6
Author(s):  
R Arun Kumar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Anesthetic Management ◽  
Surgical Excision ◽  
Cardiovascular Complications ◽  
Palpable Mass ◽  
Complete Surgical Excision ◽  
Rare Case Report ◽  
Male Preponderance ◽  
Sporadic Tumors

Paragangliomas are rare tumors derived from the neural crest cells. Most of the paragangliomas occur as sporadic tumors. The commonest incidence occurs in the second and third decade of life with a slight male preponderance. Clinically patients with a retroperitoneal paraganglioma often present with back pain or a palpable mass. There is a 5% incidence of turning into malignancy and these tumors are associated with a high risk of morbidity and mortality from cardiovascular complications. Management for paragangliomas typically involves complete surgical excision. A multi-disciplinary approach is suggested for a better outcome of the procedure

Linezolid Induced Skin Reactions in a Multi Drug Resistant Infective Endocarditis Patient: A Rare Case

2020 ◽  
Vol 15 (3) ◽  
pp. 222-226 ◽  
Author(s):  
Asha K. Rajan ◽  
Ananth Kashyap ◽  
Manik Chhabra ◽  
Muhammed Rashid
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Rare Case ◽  
Case Reports ◽  
Multidrug Resistant ◽  
The Body ◽  
Prior History ◽  
Skin Reactions ◽  
Rare Case Report ◽  
Multiple Drugs

Rationale: Linezolid (LNZ) induced Cutaneous Adverse Drug Reactions (CADRs) have rare atypical presentation. Till date, there are very few published case reports on LNZ induced CADRs among the multidrug-resistant patients suffering from Infective Endocarditis (MDR IE). Here, we present a rare case report of LNZ induced CARs in a MDR IE patient. Case report: A 24-year-old female patient was admitted to the hospital with chief complaints of fever (101°C) associated with rigors, chills, and shortness of breath (grade IV) for the past 4 days. She was diagnosed with MDR IE, having a prior history of rheumatic heart disease. She was prescribed LNZ 600mg IV BD for MDR IE, against Staphylococcus coagulase-negative. The patient experienced flares of cutaneous reactions with multiple hyper-pigmented maculopapular lesions all over the body after one week of LNZ therapy. Upon causality assessment, she was found to be suffering from LNZ induced CADRs. LNZ dose was tapered gradually and discontinued. The patient was prescribed corticosteroids along with other supportive care. Her reactions completely subsided and infection got controlled following 1 month of therapy. Conclusion: Healthcare professionals should be vigilant for rare CADRs, while monitoring the patients on LNZ therapy especially in MDR patients as they are exposed to multiple drugs. Moreover, strengthened spontaneous reporting is required for better quantification.

scholarly journals Solitary submandibular soft tissue osteochondroma: A rare case report

2021 ◽  
pp. 106074
Author(s):  
Abdulrahman Z. Nakshabandi ◽  
Ahamd F. Alomar ◽  
Moayad Baazeem ◽  
Abdulrahman Alosaimi ◽  
Ibrahim O. Bello
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Cerebral Coenurosis Masquerading as Malignancy: A Rare Case Report from India

2019 ◽  
Vol 10 (02) ◽  
pp. 367-370
Author(s):  
Shamila Mohamed Ali ◽  
P. Somashekara Reddy ◽  
S. Venugopal ◽  
Manmeet Chhabra ◽  
Anita Mahadevan
Keyword(s):  
Case Report ◽  
Characteristic Feature ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Hydatid Cysts ◽  
The Third ◽  
Rare Case Report ◽  
Cerebral Coenurosis ◽  
Cuticular Layer

ABSTRACTHuman coenurosis is a rare zoonotic disease caused by the larvae of Tinea multiceps seen in sheep-rearing countries. We report the case of a 63-year-old male who was referred to our hospital with a working diagnosis of skull base chondrosarcoma. Histopathological examination after surgical excision revealed characteristic feature of coenurus with multiple scolices invaginating from the outer cuticular layer. Coenuri are often mistaken for giant cysticercal cysts and hydatid cysts. Despite its wide prevalence in cattle, only two cases of human coenurosis are reported from India till date. We report the third case from India.

scholarly journals LIPOSARCOMA OF SPERMATIC CORD PRESENTING AS INDIRECT INGUINAL HERNIA- A RARE CASE REPORT

2011 ◽  
Vol 01 (01/03) ◽  
pp. 63-65
Author(s):  
Padma Shetty K. ◽  
Harish S. Permi ◽  
Michelle Mathias ◽  
Kishan Prasad ◽  
Teerthanath S. ◽  
...  
Keyword(s):  
Case Report ◽  
Inguinal Hernia ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Myxoid Liposarcoma ◽  
Clinical Findings ◽  
Inguinal Region ◽  
Indirect Inguinal Hernia ◽  
Rare Case Report

AbstractLiposarcoma in the inguinal region though rare are clinically significant lesions. Preoperative diagnosis is difficult since the clinical findings are very similar to that of inguinal hernia. We report a rare case of Liposarcoma of the spermatic cord in 85 year old male, clinically diagnosed as left sided indirect inguinal hernia. Surgical excision specimen showed multiple globular lipomatous masses which were yellowish and grey tan with areas of myxoid degeneration and necrosis seen. Microscopic examination showed adipocytes arranged in lobules with numerous blood vessels, lipoblasts and myxoid stroma confirming the diagnosis of myxoid liposarcoma. He is on regular follow up since two years without any recurrence or metastasis. Our case report highlights the importance of sampling and examination of fatty masses in the inguinal region to rule out the possibility of liposarcoma as they are mistaken for lipoma at surgery.

Pulmonary Carcinosarcoma with Metastasis to Soft Tissue- A Rare Case Report

2019 ◽  
Author(s):  
M.R. Malekzadegan ◽  
K. Solanki ◽  
S.H.A. Pir ◽  
T.M. Arab ◽  
S. Chauhan ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Rare Case Report ◽  
Pulmonary Carcinosarcoma
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