scholarly journals Trichilemmal Cyst of the Eyelid: Masquerading as Recurrent Chalazion

2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Manju Meena ◽  
Ruchi Mittal ◽  
Debarati Saha
Keyword(s):  
Differential Diagnosis ◽  
Postoperative Period ◽  
Rare Case ◽  
Excisional Biopsy ◽  
Lower Eyelid ◽  
Wide Excision ◽  
Histopathological Findings ◽  
Trichilemmal Cyst ◽  
History Of ◽  
One Year

A 52-years-old female presented with a history of a painless, progressive swelling in the left lower eyelid of one-year duration. The lesion was excised twice as a chalazion and recurred. Excisional biopsy of the mass was performed and histopathological findings were consistent with those of trichilemmal cyst. We report a rare case of trichilemmal cyst of the eyelid which was masquerading as chalazion for which the patient had undergone multiple surgeries. Wide excision was done and diagnosis was confirmed on histopathology. There was no recurrence seen till 2 months of postoperative period. Trichilemmal cyst, although rare, should be considered as differential diagnosis of recurrent chalazion.

Primary B-cell lymphoma presenting as bilateral ear lobule swelling

2007 ◽  
Vol 121 (12) ◽  
pp. 1207-1209 ◽  
Author(s):  
A K Sharma ◽  
S Chatterjee ◽  
V L Sharma
Keyword(s):  
B Cell ◽  
Rare Case ◽  
Cell Lymphoma ◽  
English Literature ◽  
B Cell Lymphoma ◽  
Excision Biopsy ◽  
History Of ◽  
One Year

AbstractWe report a rare case of primary B-cell lymphoma presenting as bilateral ear lobule swelling. A 56-year-old white man presented with a one-year history of painless swelling of both ear lobules. An excision biopsy confirmed B-cell lymphoma. Detailed systemic investigation confirmed the primary nature of the tumour. This tumour is rare in the ear lobule. A review of the English literature revealed no previously reported case of bilateral primary ear lobule involvement. Clinicians should be aware that this tumour can present as a primary in the ear lobules.

scholarly journals Macroglossia reveals multiple myeloma

2021 ◽  
Vol 7 (3) ◽  
Author(s):  
Maria Bonvicini ◽  
Davide Crapanzano ◽  
Susanna Fenu ◽  
Marco Giordano ◽  
Lorenzo Palleschi
Keyword(s):  
Multiple Myeloma ◽  
Bone Marrow ◽  
Differential Diagnosis ◽  
Arterial Hypertension ◽  
Supportive Care ◽  
Loss Of Weight ◽  
Bright Orange ◽  
History Of ◽  
Congo Red Staining ◽  
One Year

We present an eighty-year old man with a one year history of progressive macroglossia, dysphagia and loss of weight. He had a medical history of arterial hypertension and prostatic hypertrophy which he had under good therapeutic control. The entire tongue was swollen, had hard solidity and was slightly painful upon palpation. A tongue biopsy revealed an amyloid deposition as it coloured bright orange-red on Congo Red staining and lead us subsequently to the diagnosis of amyloidosis; then a bone marrow biopsy confirmed the diagnosis of multiple myeloma. The case was further evaluated by a multidisciplinary team who considered it appropriate to start a lowdose melphalan treatment combined with supportive care. When macroglossia in the tongue is confirmed to be amyloidosis the differential diagnosis should include systemic amyloidosis deposition and multiple myeloma.

scholarly journals Epithelioid Hemangioma of Lingual Alveolar Mucosa: An Immunohistochemical Case Report

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Rajat Nangia ◽  
Abhiney Puri ◽  
Rakhi Gupta ◽  
Sucheta Bansal ◽  
Amita Negi ◽  
...  
Keyword(s):  
Rare Case ◽  
Neck Region ◽  
Excisional Biopsy ◽  
Vascular Lesion ◽  
Histopathological Diagnosis ◽  
Epithelioid Cells ◽  
Head And Neck Region ◽  
Epithelioid Hemangioma ◽  
Exact Etiology ◽  
History Of

Epithelioid hemangioma is a rare benign vascular lesion that presents as a nodular lesion in the skin of head and neck region. It is a superficial vascular entity which can either be due to tumor or reactive lesion, but the exact etiology is still unknown. We hereby present a rare case which has been reported with the history of small nodular-like growth on mandibular buccal and lingual area. The excisional biopsy was performed and tissue was submitted for histopathological diagnosis. The immunohistochemistry was performed to check the expression of CD31 marker which proved that origin of epithelioid cells was vascular.

scholarly journals A Rare Case of Acute Renal Failure Secondary to Rhabdomyolysis Probably Induced by Donepezil

2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Osman Zikrullah Sahin ◽  
Teslime Ayaz ◽  
Suleyman Yuce ◽  
Fatih Sumer ◽  
Serap Baydur Sahin
Keyword(s):  
Emergency Department ◽  
Renal Failure ◽  
Creatine Kinase ◽  
Acute Renal Failure ◽  
Rare Case ◽  
Laboratory Studies ◽  
Case Presentation ◽  
History Of ◽  
One Year ◽  
Renal Function Tests

Introduction. Acute renal failure (ARF) develops in 33% of the patients with rhabdomyolysis. The main etiologic factors are alcoholism, trauma, exercise overexertion, and drugs. In this report we present a rare case of ARF secondary to probably donepezil-induced rhabdomyolysis.Case Presentation. An 84-year-old male patient was admitted to the emergency department with a complaint of generalized weakness and reduced consciousness for two days. He had a history of Alzheimer’s disease for one year and he had taken donepezil 5 mg daily for two months. The patient’s physical examination revealed apathy, loss of cooperation, and decreased muscle strength. Laboratory studies revealed the following: urea: 128 mg/dL; Creatinine 6.06 mg/dL; creatine kinase: 3613 mg/dL. Donepezil was discontinued and the patient’s renal function tests improved gradually.Conclusion. Rhabdomyolysis-induced acute renal failure may develop secondary to donepezil therapy.

scholarly journals A rare case of acrochordon of external auditory canal

2020 ◽  
Vol 6 (11) ◽  
pp. 2119
Author(s):  
Chandre Gowda Bendiganahalli Venkate Gowda ◽  
Rakshita R. Kamath
Keyword(s):  
Differential Diagnosis ◽  
External Auditory Canal ◽  
Rare Case ◽  
Neck Region ◽  
Excisional Biopsy ◽  
Rare Entity ◽  
Head And Neck Region ◽  
Polypoidal Growth ◽  
The Right ◽  
The Masses

<p class="abstract">Independently arising acrochordon of the external auditory canal is a rare entity with only one reported case in literature. We present here the second such case. A 54-yr old lady presented to our outpatient department with complains of aural fullness and reduced hearing in right ear for 2 weeks. Clinical examination showed a pedunculated polypoidal growth in the external auditory canal. Excisional biopsy and histopathology revealed an acrochordon. Following the procedure, patient was free of symptoms and all structures of the right ear were normal. In the head and neck region, acrochordons have only but once been reported in the external auditory canal and hence should be considered as a differential diagnosis in the masses of this region. Resection must be done for confirmation of diagnosis, differentiation from neoplasia and alleviation of symptoms when associated.  </p>

scholarly journals Schwannoma of upper eyelid: A rare differential diagnosis of eyelid swellings

2010 ◽  
Vol 43 (02) ◽  
pp. 213-215
Author(s):  
Surendra B. Patil ◽  
Satish M. Kale ◽  
Sumeet Jaiswal ◽  
Nishant Khare
Keyword(s):  
Differential Diagnosis ◽  
Lower Eyelid ◽  
Lateral Part ◽  
Upper Eyelid ◽  
Eyelid Skin ◽  
Rare Differential Diagnosis ◽  
History Of ◽  
Upper Lid ◽  
Painless Mass ◽  
Rare Benign Tumour

ABSTRACTSchwannoma is a relatively rare benign tumour of peripheral nerve origin. The occurrence of Schwannoma in eyelid is extremely rare. As per our knowledge, only 11 such cases have been reported in the literature so far. We present a case of a 40-year-old man who presented to us with a 2-year history of slowly enlarging, painless mass in his left upper lid with resultant progressive ptosis. Ocular examination was suggestive of a firm, non-tender nodule of size 2 × 1.5 × 1 cm on the left upper lid. The mass was non-adherent to the skin or the underlying tissue. The eyelid skin and conjunctiva were indurated and signs of inflammation were present. The lateral part of eyelid showed presence of an ulcer and the lid function was severely hampered. Provisional clinical diagnosis was that of an eyelid malignancy. With this in mind, the medial part of the lid was excised and reconstructed using a tarso-conjunctival flap from the lower eyelid in conjunction with a skin graft. The histopathology and immunohistochemistry established the diagnosis of Schwannoma. We recommend that Schwannoma be considered in the differential diagnosis of well-circumscribed eyelid swellings.

scholarly journals Composite paraganglioma-ganglioneuroma of the urinary bladder: a rare neoplasm causing hemodynamic crisis at tumour resection

2013 ◽  
Vol 3 (5) ◽  
pp. 45 ◽  
Author(s):  
C-H. Chen ◽  
Alexander H. Boag ◽  
Darren T. Beiko ◽  
Robert Siemens ◽  
Alison Froese ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Urinary Bladder ◽  
Transurethral Resection ◽  
Bladder Neck ◽  
Neck Mass ◽  
Tumour Resection ◽  
History Of ◽  
Primary Bladder ◽  
One Year ◽  
Normal Urothelium

A 64-year-old man presented with gross painless hematuria.Cystoscopy revealed a submucosal bladder neck mass coveredby normal urothelium. During transurethral resection, the patientdeveloped hemodynamic crisis including sinus bradycardia.Histopathologic examination revealed a primary bladder compositeparaganglioma-ganglioneuroma (CPG). The patient underwentpartial cystectomy and is symptom-free after one year. BladderCPGs are extremely rare neoplasms that may result in lifethreateningcatecholamine secretion, especially during tumourmanipulation. These tumours require complete surgical excisionand should be included in the differential diagnosis of any solitarybladder mass covered by normal urothelium, especially whenthere is a history of hypertension or micturition attacks.

scholarly journals Esophageal Pharmacobezoar in a Patient with Achalasia: A Case Report

2019 ◽  
Vol 11 (3) ◽  
pp. 174-176 ◽  
Author(s):  
Hamid Tavakkoli
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Ferrous Sulfate ◽  
Rare Case ◽  
Distal Part ◽  
Balloon Dilation ◽  
Barium Swallow ◽  
Severe Dysphagia ◽  
History Of ◽  
Black Color

A few cases with esophageal bezoar have been reported in achalasia. We describe here a rare case of esophageal pharmacobezoar after ingestion of ferrous sulfate capsules in a patient with achalasia. A 29-year-old woman presented with severe dysphagia since five days earlier. She had history of achalasia since 3 years ago but had refused any treatment option. After about 3 weeks of ferrous sulfate capsules ingestion, she developed severe dysphagia and was referred to a gastroenterologist. Physical examination was unremarkable. A barium swallow revealed dilated esophagus and bird’s beak appearance. Esophagogastroduodenoscopy (EGD) showed dilated esophagus and soft black color bezoar in distal part of esophagus. The bezoar was retrieved with basket. In the next endoscopic session, achalasia balloon dilation was successfully applied. Ferrous sulfate capsules can cause pharmacobezoar in patients with achalasia. Esophageal bezoar should be considered in differential diagnosis of untreated achalasia and acute exacerbation of dysphagia.

scholarly journals Scrotal Peripheral Primitive Neuroectodermal Tumor

2018 ◽  
Vol 12 (1) ◽  
pp. 50-53 ◽  
Author(s):  
Sandra Baleato-González ◽  
Maria Gabriela Tirapu-de-Sagrario ◽  
Elena Pintos-Martínez ◽  
Roberto García-Figueiras
Keyword(s):  
Differential Diagnosis ◽  
Molecular Imaging ◽  
Malignant Tumor ◽  
Rare Case ◽  
Primitive Neuroectodermal Tumor ◽  
Neuroectodermal Tumor ◽  
Pelvic Cavity ◽  
Peripheral Primitive Neuroectodermal Tumor ◽  
Chest Cavity ◽  
History Of

The peripheral primitive neuroectodermal tumor (pPNET) is a rare malignant tumor originating from neuroectoderm that usually occurs in children or adolescent and is frequently located in the extremities, chest cavity, pelvic cavity and chest wall. We present a rare case of an 84-year-old man with a history of pPNET in the scrotal sac, to our knowledge not previously published in the literature. The presence of a large irreducible mass in the inguinal sac forced to exclude a tumor. Ultrasound and MRI are very useful modalities to assess the location of the mass, its dependency from any organ and the tumoral internal structure. Molecular imaging with the detection of EWS-FLI1 fusion transcripts is useful for the diagnosis and differential diagnosis of Ewing sarcoma/pPNETs.

scholarly journals Angiosarcoma of the nasal cavity and paranasal sinuses: a rare case report

2017 ◽  
Vol 3 (3) ◽  
pp. 735
Author(s):  
Jyoti Singh ◽  
Jai Lal Davessar ◽  
Sumit Prinja ◽  
Nitin Arora
Keyword(s):  
Paranasal Sinuses ◽  
Rare Case ◽  
Excisional Biopsy ◽  
Surgical Removal ◽  
Left Nostril ◽  
Vascular Phenotype ◽  
Rare Case Report ◽  
History Of ◽  
Poorly Differentiated ◽  
Nose And Paranasal Sinuses

<p class="abstract">Angiosarcomas are the malignant neoplasias of vascular phenotype whose constituent tumor cells have endothelial features. They account for less than 1% of all sinonasal tract malignancies. A case of 65 year old male with a 6 months history of spontaneous epistaxis and a nasal mass lesion presented to the OPD. On physical examination, a polypoidal purplish tumor of 6 × 5 cm was identified. A NCCT scan of nose and paranasal sinuses showed a nonenhanced tumor in the left nostril in maxillary, ethmoid, sphenoid and frontal sinus. An excisional biopsy revealed a poorly differentiated angiosarcoma. Surgical removal of the lesion was advised which was refused by the patient.</p><p class="abstract">Patient was put on the radiation therapy. Angiosarcoma of the nose and paranasal sinuses is an extremely rare tumor. Recurrences are common due to incomplete excision or mutiflocality.</p>

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