O10 GIANT ESOPHAGEAL POLYP PROTRUDING THROUGH THE MOUTH: A RARE CASE

2019 ◽  
Vol 32 (Supplement_2) ◽  
Author(s):  
I Tsomidis ◽  
G Kalopitas ◽  
K Dinaki ◽  
G Germanidis ◽  
J Constantinidis

Abstract Aim Giant esophageal polyps are a relative rare and benign entity, which can lead to major complications. Our knowledge about their pathology and management originates from scattered case reports. Our aim is to report the clinical presentation and management of this rare case in order to enrich the current literature. Background & Methods Large pedunculated esophageal polyps are a rare entity encountered in clinical practice. The majority of these polyps are located near the upper esophageal sphincter or upper esophagus. They are slowly growing and asymptomatic. Most common clinical symptoms, associated with polyp size, include dysphagia, chest pain, regurgitation and, rarely, acute respiratory distress. Histology reveals benign submucosal tumors with fibrous and vascular components, covered by normal squamous cells, in most cases. Malignant transformation of these polyps has been infrequently described. Surgical approach, either with endoscopic resection or with open surgery, is the treatment of choice and recurrence is extremely uncommon. A review of current literature was conducted, followed by presentation of our rare case. Results A 50 year-old woman with clear medical history presented with a 3-month history of dysphagia and endoscopy revealed a large esophageal polyp extending from the upper esophageal sphincter to the lower esophageal sphincter. The initial attempt of endoscopic resection of the polyp led to regurgitation and intraoral prolapse of the polyp, causing respiratory distress. The patient was transferred to the ENT operation room and an orotracheal intubation was performed. The tumor was successfully removed transorally after ligation of its stem. Histopathology showed an inflammatory fibroid polyp (IFP) and postsurgical follow-up revealed no recurrence of the mass. Conclusion Giant IFPs are an extremely rare entity among upper esophageal polyps and the pathogenesis of these tumors remains poorly understood. Life threatening regurgitation of the polyp causing respiratory distress is an uncommon complication demanding urgent surgical approach. Once diagnosed, these benign tumors can be removed either with open surgery or endoscopic resection depending on the location and the size of the tumor. The impressive size of these polyps renders them a challenge for surgeons and endoscopists, whose cooperation is often in need.

2019 ◽  
Vol 6 (12) ◽  
pp. 4583
Author(s):  
Nishanth S. ◽  
Sudhir Kumar Jain ◽  
Chandra Bhushan Singh

Achalasia cardia is a primary motility disorder of esophagus which is due to loss of ganglion cells in myentric plexus, etiology of which is unknown. The condition causes dysphagia due to failure of relaxation of lower esophageal sphincter. Pseudoachalasia is a similar disorder which occurs usually due to adenocarcinoma of the cardia and also due benign tumors at this level. We present a rare case of pseudocyst of pancreas extending into mediastinum which mimics as pseudoachalasia.


2021 ◽  
pp. 014556132110181
Author(s):  
Maria Garefi ◽  
Konstantinos Garefis ◽  
Vasilios Nikolaidis ◽  
Angelos Chatziavramidis ◽  
Iordanis Konstantinidis ◽  
...  

Hemangiomas of the head and neck account for about 7% of all benign tumors in children. Τhey are rare in the nasal cavity and especially in the nasal septum. Only 16 cases of intranasal hemangiomas in childhood have been previously described in the literature and 6 of them arising from the nasal septum. We present a rare case of a nasal septum hemangioma (NSH) in a 9-year-old boy who was treated with transnasal endoscopic resection.


2010 ◽  
Vol 1 (1) ◽  
pp. 21-24
Author(s):  
D'Cruz Anil ◽  
Dandekar Mitali ◽  
Chaukar Devendra ◽  
Kane Shubhada ◽  
Juvekar Shashikant

Abstract Objective Rare case of intracapsular carcinoma ex pleomorphic adenoma in the buccal space with focus on its appropriate management. Method Case report with review of current literature on buccal space lesions and intracapsular carcinoma ex pleomorphic adenoma. Result Although salivary gland tumors are common, intracapsular carcinoma ex pleomorphic adenoma is a rare entity especially within the buccal space with no similar case report in the current literature. Conclusion Our case is unusual due to its unusual presentation in the buccal space and pathological features. This case report also highlights issues regarding its appropriate management.


Author(s):  
Abhinav Sharma

Background: Minor salivary gland benign tumors account for a very small percentage of salivary gland tumors of which monomorphic adenomas are a rare entity. Methods and Findings: The present case report discusses a rare case report of an 18-year-old female patient diagnosed with monomorphic adenoma of the posterior palatal region. The diagnosis was reached after thorough radiographical and pathological investigations. Conclusion: Monomorphic Adenoma in a younger individual is a rare disorder and can be used as a collective term for benign or malignant tumors comprising of one type or even two types of cells.


Author(s):  
Vikram K. Bhat ◽  
Supreetha B. Shenoy ◽  
Bhavana Sangoli

<p class="abstract"><span lang="EN-IN">Pleomorphic adenomas are benign tumors that are uncommon in the nasal cavity. However, they can rarely arise from septum, erode hard palate and thus masquerade a bone tumor. We report one such rare case of septal pleomorphic adenoma with hard palatal extension and ossification. A combined endoscopic intranasal and transpalatal surgical approach was performed and tumor was excised completely. A high index of clinical suspicion and biopsy can diagnose such swellings.</span></p>


Author(s):  
K. V. Lokanath ◽  
Debaditya Basu ◽  
Abhinav Kuthiala

<p class="abstract">Osteomas are benign mesenchymal osteoblastic tumors of lamellar bones. In our practice, they are usually seen in the paranasal sinuses, mainly involving the frontal and ethmoidal sinus. Osteoma of the temporal bone is uncommon and when they occur, they are most commonly seen in the external auditory canal. Mastoid osteomas are a rare entity with incidence of 0.1 - 1% of all benign tumors of skull. They are slowing growing and usually asymptomatic. We report a rare case in a 28 years female patient who presented to us with right postauricular bony swelling of size 2.5×3 cms along with bilateral nasal obstruction. Patient was analyzed for her clinical condition, imaging details, treatment and surgical plan. Diagnosis of right mastoid osteoma with right nasochoanal polyposis was made after non-contrast computed tomography of temporal bone and paranasal sinuses respectively. Complete surgical excision of the osteoma along with endoscopic removal of the polypoidal tissue was done with good cosmetic outcome without recurrence.</p>


2020 ◽  
Vol 3 (2) ◽  
pp. 56-58
Author(s):  
Bittmann Stefan ◽  
◽  
Luchter Elisabeth ◽  
Moschüring-Alieva Elena ◽  
Villalon Gloria ◽  
...  

We report the case of a 6-year-old boy with dysphagia and iron deficiency anemia with an Hb of 5.6 g/dl leading the diagnosis of Plummer-Vinson syndrome. An esophageal stenosis of 4 mm diameter near the upper esophageal sphincter was found. Balloon dilatation and iron substitution cured the problem. Pediatricians should keep in mind that the rare entity of Plummer-Vinson syndrome in unclear cases of dysphagia.


2021 ◽  
pp. 175857322110273
Author(s):  
Youval Lotan ◽  
Ahmad Essa ◽  
Naser Haj Yaseen ◽  
Eran Tamir ◽  
Nir Golan ◽  
...  

Locked scapula or intrathoracic scapular dislocation is an extremely rare entity encountered in the emergency department, with very few cases reported in literature. Conservative vs surgical approach in treating intrathoracic scapular dislocation is not well defined in literature. In this case report, we present a rare case of intrathoracic scapular dislocation, following multiple ribs resection due to malignant bone tumour, which was treated by closed manipulation reduction technique.


JMS SKIMS ◽  
2011 ◽  
Vol 14 (1) ◽  
pp. 28-29
Author(s):  
R K Maurya ◽  
Pawan Kumar Singh ◽  
Sandeep Singh

Lipomas of vulva have been reported only rarely. Benign tumors of the vulva are normally classified according to their origin as epithelial cell tumors (e.g., keratinocytic, adnexal and ectopic tumors), or mesenchymal cell tumors (e.g., vascular, fibrous, muscular, neural, adipose and melanocytic tumors). Vulvar lipomas need to be differentiated from liposarcomas, which are rare but are very similar to lipomas clinically. Here we present a rare case of large vulvar lipoma in an adolescent girl. JMS 2011;14(1):28-29


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