scholarly journals Rare case of intra-oral palatal (soft palate) fibro-lipoma

2021 ◽  
Author(s):  
Manit Mandal ◽  
Ajay Panchal ◽  
Rakesh Kumar ◽  
Parth Kapadia ◽  
Neel Parmar
Keyword(s):  
Soft Palate ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Combined Approach ◽  
Complete Evaluation ◽  
Endoscopic Excision

Background: Case study of 30 years male having suspending mass found over upper surface of soft palate hanging in nasopharynx. Methods: After evaluation, patient underwent combined approach (Trans-oral + Endoscopic) excision. Results: Histopathological examination concluded possibility of intra-oral lipoma. Conclusion: Palatal mass (lipoma) requires surgical excision post complete evaluation.

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 A rare case of concomitant bilateral nipple and vulval condyloma accuminatum

2019 ◽  
Vol 7 ◽  
pp. 2050313X1881962 ◽  
Author(s):  
Langanani Mbodi ◽  
Trudy Smith ◽  
Reubina Wadee
Keyword(s):  
Human Papillomavirus ◽  
Antiretroviral Therapy ◽  
Direct Contact ◽  
Rare Case ◽  
Surgical Excision ◽  
Low Risk ◽  
Hiv Positive ◽  
Human Papillomavirus Infection ◽  
Papillomavirus Infection

In this case study, we have presented a rare case of concomitant human papillomavirus condylomata lesions of both breast nipples and giant vulval warts in an HIV-positive woman on antiretroviral therapy. The woman underwent successful surgical excision and reconstruction for both breast nipple condylomata and vulval warts. Histology of the excised breast nipple and vulval tissue confirmed low-risk human papillomavirus infection. Concomitant vulval and bilateral breast nipple condylomata pose a management dilemma. It is possible that the pathogenesis of these lesions is through both direct contact spread as well as haematogenous dissemination of the human papillomavirus.

Neurofibroma of Soft Palate: A Rare Case Report

2013 ◽  
Vol 5 (2) ◽  
pp. 19-20
Author(s):  
SG Smitha ◽  
Smitha Soubhagya Gangaraj ◽  
Lakshmi Shantharam ◽  
Suguna Vijay
Keyword(s):  
Case Report ◽  
Soft Palate ◽  
Rare Case ◽  
Histopathological Examination ◽  
English Literature ◽  
Rare Tumor ◽  
Fourth Case ◽  
Intraoral Approach ◽  
Rare Case Report

ABSTRACT Neurofibroma of soft palate is a rare tumor with this report being the fourth case reported in English literature. We are reporting this case of isolated neurofibroma of soft palate for its rarity. The mass was excised by intraoral approach without prior tracheostomy. Histopathological examination showed features of neurofibroma with secondary changes.

scholarly journals Rare case of intra-oral palatal (soft palate) fibro-lipoma

2021 ◽  
Vol 7 (5) ◽  
pp. 885
Author(s):  
Manit M. Mandal ◽  
Ajay J. Panchal ◽  
Rakesh Kumar ◽  
Parth B. Kapadia ◽  
Neel Parmar
Keyword(s):  
Differential Diagnosis ◽  
Oral Cavity ◽  
Nasal Obstruction ◽  
Male Patient ◽  
Soft Palate ◽  
Rare Case ◽  
Endoscopic Examination ◽  
Chief Complaints ◽  
Dual Route

<p>Amongst various differential diagnoses possible for intra-oral (palatal) mass, possibility of fibro-lipoma is extremely rare but documented in literature, and hence should be a consideration. Such patient requires thorough evaluation and step-wise approach to treat. This case study documents for a 30-year-old male patient presenting with such mass and chief complaints of post nasal drip, nasal obstruction (right side&gt;left side) and intermittent headache for 3 years. After radiological and endoscopic examination, the mass was surgically removed in toto via dual route (trans-oral and endoscopic).  Lipomas are uncommon tumors in the oral cavity, and palate being the rarest amongst them as is our case. It would be strongly advocated to keep lipoma in the differential diagnosis when evaluating a palatal mass. Also, it is worth mentioning and recommending that a careful radiological examination of large lesions arising from the palate is a must before approaching for surgery.</p>

scholarly journals A rare case of Kimura lymphadenpathy in elderly female

2020 ◽  
Vol 7 (10) ◽  
pp. 3452
Author(s):  
Vinayagam Ganesan ◽  
Venkatesh Sadayan Periyasamy ◽  
Muralidharan Kannaian
Keyword(s):  
Rare Case ◽  
Immunoglobulin E ◽  
Histopathological Examination ◽  
Renal Involvement ◽  
Cervical Lymphadenopathy ◽  
Surgical Excision ◽  
Excision Biopsy ◽  
Kimura’S Disease ◽  
Recurrence Rates ◽  
Elderly Female

Kimura's disease (KD) is a chronic inflammatory disease, a rare variety. It usually presents as non-tender subcutaneous swelling in head and neck region, predominantly in preauricular and submandibular area and is often associated with cervical lymphadenopathy, marked peripheral eosinophilia and an elevated immunoglobulin E (IgE) level. Renal involvement is the only systemic manifestation.4 Nephrotic syndrome is the most common manifestation of renal disease in KD. Diagnosis through Fine needle aspiration cytology (FNAC) is misleading and can easily be mistaken as a malignant disease. So, diagnosis is therefore only established by histopathological examination. The treatment of KD involves one of three major approaches are surgical excision, irradiation, or steroid therapy. Surgical excision is recommended as the treatment of choice but carries recurrence rates of 33-50%. In our study, we are reporting a case of elderly female who presented with left sided cervical lymphadenopathy for which excision biopsy was done and the histopathology examination shown as kimura lymphadenopathy, a rare case.

scholarly journals Functional and Esthetic Correction of Severe Localized Pregnancy-Induced Gingival Enlargement associated with Capillary Hemangioma

2017 ◽  
Vol 1 (8) ◽  
pp. 248-251
Author(s):  
Pawan Kumar ◽  
Saindhya Tora Sonowal ◽  
Jitu Chawla
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Immunological Response ◽  
Surgical Excision ◽  
Capillary Hemangioma ◽  
Anterior Maxilla ◽  
Attached Gingiva ◽  
Gingival Enlargement ◽  
Rare Case Report

Gingival enlargement is a clinical condition that has been directly associated with specific local or systemic conditions. Pregnancy has been considered an attributing factor which increases the susceptibility to gingival enlargement. It is also considered as a risk factor for periodontitis because of its ability to allow proliferation of specific microorganisms and affect host immunological response. This paper presents a rare case report of capillary hemangioma on attached gingiva of anterior maxilla in an adult female which initiated when she was in her 10th week of gestation. After parturition, gingival enlargement further progressed and caused functional and aesthetic problem. Enlargement did not resolve even after non-surgical therapy; therefore, surgical excision of the entire enlargement was preformed. Histopathological examination revealed capillary hemangioma. No evidence of malignancy was seen. No recurrence was seen even after 2 years of follow-up.

Rare case of a massive buccal mucocele

Open Medicine ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. 305-308
Author(s):  
Rafał Koszowski ◽  
Jadwiga Waśkowska ◽  
Tadeusz Morawiec ◽  
Sylwia Wojcik ◽  
Katarzyna Stęplewska
Keyword(s):  
Oral Cavity ◽  
Rare Case ◽  
Clinical Symptoms ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Facial Injury ◽  
Pathological Lesions ◽  
Preoperative Ultrasonography

AbstractMucoceles are common pathological lesions of the oral cavity, usually measuring up to 10 mm. The authors describe a case of deeply located buccal mucocele measuring 35 mm in diameter. The lesion was caused by facial injury in a 54-year old man. The lesion persisted for approximately 2.5 years and was difficult to diagnose because of its unusual size and atypical clinical symptoms. Preoperative ultrasonography excluded a tumor, and this was confirmed by histopathological examination. However, oncological alertness was considered necessary on account of ulcerated mucosa next to the lesion. The mucocele was removed through surgical excision, using a scalpel and tissue scissors. No recurrence was observed in 2.5 postoperative years. It is stressed that histopathological examinations help to differentiate mucoceles from other disease processes.

scholarly journals Rudimentary Meningocele of the Scalp: A Pitfall in the Diagnosis of Vascular Neoplasms

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Subramaniam Ramkumar
Keyword(s):  
Soft Tissue ◽  
Rare Case ◽  
Histopathological Examination ◽  
Subcutaneous Tissue ◽  
Surgical Excision ◽  
Endothelial Markers ◽  
Vascular Neoplasms ◽  
Soft Tissue Swelling ◽  
Ct Brain ◽  
Dermal Lesion

We present a case of sequestrated meningocele in a 1-year-old girl, who presented with a 1x1cm occipital swelling since birth. CT brain revealed the soft tissue swelling to be extracranial. She underwent surgical excision of the specimen and the excised mass was sent for histopathological examination. The specimen consisted of skin and subcutaneous tissue measuring 2 x 1 x 1 cm. The entire tissue was paraffin processed. Multiple sections studied from the lesion showed an ill circumscribed locally infiltrative dermal lesion. The lesion was composed of whorled proliferations of meningothelial cells enclosing pseudovascular spaces. Immunohistochemically the lesion was positive for EMA, Desmin, and negative for endothelial markers. The present case was documented as a rare case of a rudimentary meningocele.

scholarly journals Rare Case of Childhood Lipoblastoma presenting as Tongue Mass

2021 ◽  
Vol 29 (1) ◽  
pp. 113-117
Author(s):  
Anand V ◽  
Aishwarya Anand ◽  
Manaswini Ramachandra ◽  
Sridurga Janarthanan
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Precise Location ◽  
Recommended Treatment ◽  
Complete Surgical Excision ◽  
Imaging Characteristics ◽  
Rare Benign Tumour ◽  
White Fat

Introduction Lipoblastoma is a rare benign tumour arising from embryonic white fat been commonly noted in limbs and trunk, but tongue involvement is rare and has not yet been reported. Case Report A child with tongue lipoblastoma is reported, whose imaging reported an encapsulated, well-delineated, fat-containing tumour. Surgical excision was performed with no post-operative morbidities.  Discussion Lipoblastoma is an uncommon childhood tumour, which rarely affects the tongue. It presents as a progressive painless swelling, rarely causing any symptom. MRI is helpful to assess the precise location and extent of the lesion. Although the ratio of fat to myxocollagenous tissue in the tumour is variable, the diagnosis can be suggested in most cases based on the imaging characteristics. Recommended treatment is complete surgical excision and confirmation of diagnosis by histopathological examination.

scholarly journals Dermal fibroma in olive barb Systomus sarana (Hamilton, 1822): a case study

2017 ◽  
Vol 64 (1) ◽  
pp. 95 ◽  
Author(s):  
M. K. Sahoo ◽  
P. Rajesh Kumar ◽  
S. Pattanayak ◽  
P. C. Das ◽  
P. K. Sahoo
Keyword(s):  
Squamous Epithelium ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
The Body ◽  
Lateral Side ◽  
Fibrous Stroma ◽  
Non Invasive ◽  
Stratified Squamous Epithelium

Systomus sarana (Hamilton, 1822) (weight; 370 g; length: 29.0 cm ) obtained from a carp polyculture pond revealed presence of a solid nodular tumorous mass on right dorso-lateral side of the body. Surgical excision and further histopathological examination of the focal non-invasive mass revealed that the tumor is a fibroma covered by thick stratified squamous epithelium. The fibroma had a compact fibrous stroma organised in whorls and bundles.

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