scholarly journals Epibulbar complex choristoma with simultaneous involvement of eyelid: a case report

2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Yun Hsia ◽  
Huang-Chun Lien ◽  
I-Jong Wang ◽  
Shu-Lang Liao ◽  
Yi-Hsuan Wei
Keyword(s):  
Case Report ◽  
Histopathological Examination ◽  
Atypical Presentation ◽  
Fundus Examination ◽  
Upper Eyelid ◽  
Case Presentation ◽  
Ectopic Cilia ◽  
The Right ◽  
Nevus Sebaceous

Abstract Background Epibulbar complex choristoma, a rare congenital epibulbar tumor, has many diverse forms. Reviewing the literature, it can present clinically as either a circumferential or isolated epibulbar mass, limbal tumor, lateral canthal mass, aggregate of ectopic cilia in the upper eyelid, eyelid mass mimicking chalazion, or lacrimal caruncle mass. The management depends on the extent of involvement, the risk of amblyopia, and cosmetic concerns. Here, we report an atypical presentation of epibulbar complex choristoma with simultaneous eyelid involvement. Case presentation A 1-month-old full-term boy was brought to our clinic with congenital epibulbar mass of the right eye with simultaneous eyelid involvement. Dilated fundus examination was unremarkable. Survey for linear nevus sebaceous Jadassohn was negative. Due to concerns of possible amblyopia and cosmetics, lamellar keratectomy, sclerotomy, and conjunctivoplasty were performed to remove the epibulbar lesion. The eyelid defect was reconstructed with 6–0 Vicryl sutures. Histopathological examination reported complex choristoma. Upon three-year follow-up, low astigmatism and favorable cosmetics results were achieved. Conclusions Congenital complex choristoma can present clinically as an epibulbar mass with eyelid involvement. The management depends on the extent of involvement, the risk of amblyopia, and cosmetic concerns. The method of eyelid reconstruction should be tailored according to the residual eyelid defect.

scholarly journals Solitary Fibrofolliculoma of the Upper Eyelid in a 68-year Old Female: A Case Report

2020 ◽  
Author(s):  
Wenqiu Wang ◽  
Jinwei Cheng
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Benign Tumor ◽  
Upper Eyelid ◽  
Solitary Lesion ◽  
Case Presentation ◽  
Multiple Lesions ◽  
Tissue Tumor ◽  
Upper Lid ◽  
The Right

Abstract Background : Fibrofolliculoma is a benign, perifollicular, connective tissue tumor, and it usually arises in the form of multiple lesions, but rarely as a solitary lesion. We report a case of solitary fibrofolliculoma on the eyelid. Case presentation: A 68-year-old female presented with an asymptomatic mass on the right upper eyelid. The lesion appeared as a flesh-colored, dome-shaped, smooth nodule being the size of 5×5×4 mm, with eyelashes protruding from the surface, and located on the upper lid margin. Shave excision was performed, and the diagnosis of fibrofolliculoma was confirmed finally through histological exam. Conclusions: Solitary fibrofolliculomas rarely arises on the eyelid. However, it should be suspected when a flesh-colored and doom-shaped lesion of the eyelid is encountered. The benign tumor on the lid margin can be removed by shave biopsy.

scholarly journals Solitary Fibrofolliculoma of the Upper Eyelid in a 68-year Old Female: A Case Report

2019 ◽  
Author(s):  
Wenqiu Wang ◽  
Jinwei Cheng
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Benign Tumor ◽  
Upper Eyelid ◽  
Solitary Lesion ◽  
Case Presentation ◽  
Multiple Lesions ◽  
Tissue Tumor ◽  
Upper Lid ◽  
The Right

Abstract Background : Fibrofolliculoma is a benign, perifollicular, connective tissue tumor, and it usually arises in the form of multiple lesions, but rarely as a solitary lesion. We report a case of solitary fibrofolliculoma on the eyelid. Case presentation: A 68-year-old female presented with an asymptomatic mass on the right upper eyelid. The lesion appeared as a flesh-colored, dome-shaped, smooth nodule being the size of 5×5×4 mm, with eyelashes protruding from the surface, and located on the upper lid margin. Shave excision was performed, and the diagnosis of fibrofolliculoma was confirmed finally through histological exam. Conclusions: Solitary fibrofolliculomas rarely arises on the eyelid. However, it should be suspected when a flesh-colored and doom-shaped lesion of the eyelid is encountered. The benign tumor on the lid margin can be removed by shave biopsy.

scholarly journals Atypical Presentation of Traumatic Neuroma: A case report

2017 ◽  
Vol 13 (3) ◽  
pp. 366-369
Author(s):  
Bela Agrawal ◽  
Ajit Kumar Yadav ◽  
Khushboo Goel ◽  
Sajeev Shrestha ◽  
Ashish Shrestha
Keyword(s):  
Case Report ◽  
Smooth Surface ◽  
Histopathological Examination ◽  
Neural Tissue ◽  
Signs And Symptoms ◽  
Mental Foramen ◽  
Atypical Presentation ◽  
Traumatic Neuroma ◽  
Reactive Proliferation

Congenital Traumatic neuroma is a rare disorder that represents a reactive proliferation of neural tissue followingdamage to an adjacent nerve. Rarely these lesions appear in the oral cavity with certain predilection for the mental foramen and the tongue area. However, its presentation on lip is more unusual with only few cases being reported in the literature. Typically diagnosed in middle-aged women, patient complains of pain as a frequent symptom. Clinically, the lip lesions appear as a normal or grayish white nodule with a smooth surface that typically resembles a mucocele. We report here a case of a 37-year old female who presented with similar signs and symptoms and was diagnosed clinically as a mucocele. However, histopathological examination revealed it as a traumatic neuroma that was surgically excised. The patient is under follow-up with no signs of recurrence for 18 months. 

scholarly journals A Case Report of Chondrosarcoma of Temporomandibular Joint

2021 ◽  
Author(s):  
Hage Ampu ◽  
Tanya Singh ◽  
Sunil Kumar ◽  
H. P. Singh ◽  
Shalini Bhalla
Keyword(s):  
Case Report ◽  
Temporomandibular Joint ◽  
Histopathological Examination ◽  
Mandibular Condyle ◽  
Joint Space ◽  
Neuralgic Pain ◽  
Well Differentiated ◽  
The Right ◽  
Disease Free

AbstractIn this case report we describe a rare case of chondrosarcoma of the Temporomandibular joint in a 70 years old female who presented with a right preauricular swelling, trismus and neuralgic pain. On examination, firm and tender swelling was noted in the right preauricular region. CT Scan revealed 3.48 × 3.0 cm size mass lesion in the region of mandibular condyle and extending into the right temporomandibular joint space. The cytopathological report was suggestive of chondroid malignancy. The tumor was excised and histopathological examination showed large sheets of atypical tumor cells with cartilaginous matrix and diagnosis of a well differentiated Chondrosarcoma was confirmed. Post-surgical resection, patient remains disease free at 15 months follow up.

scholarly journals Malignant Mesothelioma of the Epididymis: A Case Report of a Rare Paratesticular Neoplasm and Literature Review

2020 ◽  
pp. 1-3
Author(s):  
Jasser Maatougui ◽  
Jasser Maatougui ◽  
Mehdi Raboudi ◽  
Tarek Taktak ◽  
Issam Msakni ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Malignant Mesothelioma ◽  
Poor Prognosis ◽  
Histopathological Examination ◽  
Multidisciplinary Management ◽  
Case Presentation ◽  
Scrotal Ultrasound ◽  
Disease Free

Background: Malignant mesothelioma of the epididymis is an extremely rare neoplasm with a poor prognosis and high potential of recurrence. Case Presentation: We report a case of a 28-year-old male with a left painless epididymal nodule. Scrotal ultrasound revealed a nodular mass with mixed echogenicity and Doppler showed increased vascularity. Radical orchidectomy was performed. Histopathological examination concluded to a malignant mesothelioma involving the epididymis. Metastatic workup was negative. The patient has undergone a regular follow-up and has been disease-free within 6 months. Conclusion: Malignant mesothelium of the epididymis is a diagnosis challenge. Surgery remains the main treatment. A multidisciplinary management should be offered in those cases.

scholarly journals Solitary Fibrofolliculoma of the Upper Eyelid in a 68-year Old Female: A Case Report

2019 ◽  
Author(s):  
Wenqiu Wang ◽  
Jinwei Cheng
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Mass Lesion ◽  
Upper Eyelid ◽  
Solitary Lesion ◽  
Case Presentation ◽  
Multiple Lesions ◽  
Tissue Tumor ◽  
Upper Lid ◽  
The Right

Abstract Background Fibrofolliculoma is a benign, perifollicular, connective tissue tumor, which is a clinically asymptomatic, 2-4 mm, skin-colored, dome-shaped smooth papule. It usually arises in the form of multiple lesions, and very rarely presents as a solitary lesion. Case presentation A 68-year-old female presented with an asymptomatic, flesh-colored mass on the right upper eyelid. The 5×5×4 mm lesion was located near upper lid margin. It was a skin-colored, dome-shaped, smooth nodule, with eyelashes on the surface, rubbery to palpation and not painful. The lesion was excised completely, and the diagnosis of fibrofolliculoma was confirmed through a histological exam. Conclusions Solitary fibrofolliculomas is rarely arising in the eyelid. However, it should be suspected when a localized mass lesion of the eyelid is encountered.

Oral Verrucous Hyperplasia: A Case Report

2019 ◽  
Vol 11 (1) ◽  
pp. 56-61
Author(s):  
Dr. Sanjeela Guru ◽  
Dr. Adithya Reddy ◽  
Dr. Shyam Padmanabhan ◽  
Dr. Rakshith Guru
Keyword(s):  
Case Report ◽  
Present Article ◽  
Histopathological Examination ◽  
Verrucous Carcinoma ◽  
Alveolar Ridge ◽  
Histopathologic Examination ◽  
Oral Mucous Membrane ◽  
Verrucous Hyperplasia ◽  
The Right

Oral Verrucous Hyperplasia is considered as an initialtype of verrucous carcinoma, representing a plausible malignant transformationof the oral mucous membrane. Studies have documented that verrucous hyperplasia transforms into verrucous carcinoma quite consistently and hence both theselesions should be managed identically. The present article reports the case of a 62-year-old male patient whoseprimary complaintwas that of a non-scrapableexophytic warty white outgrowth on edentulous alveolar ridge in the right upper posterior tooth region of the jaw. The growth was provisionally diagnosed as Squamous papilloma. Excision of the exophyticlesion was doneand the tissue biopsy sent for histopathological examination. Histopathologic examination suggested that the lesion was Oral Verrucous hyperplasia. 3 month follow-up of the patient revealed no signs of recurrence.

scholarly journals Solitary Fibrofolliculoma of the Upper Eyelid in a 68-year Old Female: A Case Report

2019 ◽  
Author(s):  
Wenqiu Wang ◽  
Jinwei Cheng
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Mass Lesion ◽  
Upper Eyelid ◽  
Solitary Lesion ◽  
Case Presentation ◽  
Multiple Lesions ◽  
Tissue Tumor ◽  
Upper Lid ◽  
The Right

Abstract Background Fibrofolliculoma is a benign, perifollicular, connective tissue tumor, which is a clinically asymptomatic, 2-4 mm, skin-colored, dome-shaped smooth papule. It usually arises in the form of multiple lesions, and very rarely presents as a solitary lesion. Case presentation A 68-year-old female presented with an asymptomatic, flesh-colored mass on the right upper eyelid. The 5×5×4 mm lesion was located near upper lid margin. It was a skin-colored, dome-shaped, smooth nodule, with eyelashes on the surface, rubbery to palpation and not painful. The lesion was excised completely, and the diagnosis of fibrofolliculoma was confirmed through a histological exam. Conclusions Solitary fibrofolliculomas is rarely arising in the eyelid. However, it should be suspected when a localized mass lesion of the eyelid is encountered.

scholarly journals Removal of hematoma due to massive hemoptysis after transbronchial biopsy: a case report

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Harushi Ueno ◽  
Hideki Tsubouchi ◽  
Keita Nakanishi ◽  
Tomoshi Sugiyama ◽  
Yuka Kadomatsu ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Transbronchial Biopsy ◽  
Massive Hemoptysis ◽  
Lobe Bronchus ◽  
Case Presentation ◽  
Life Threatening ◽  
Life Threatening Complication ◽  
The Right

Abstract Background Massive hemoptysis is a life-threatening complication after transbronchial biopsy (TBB). Reports on massive hemoptysis occurring several days after TBB are scarce. Case presentation A 62-year-old man presented with massive hemoptysis and was admitted to hospital as an emergency on the eighth day after TBB. On the 12th day after TBB, computed tomography showed complete atelectasis of the right middle and lower lobes. The patient underwent emergent right upper lobectomy. The right upper lobe bronchus was separated with a scalpel, the hematoma was pulled out with forceps, and the bronchus subsequently sutured shut. The patient was discharged from the hospital uneventfully. Conclusions We experienced a case of massive hemoptysis on the eighth day after TBB, which required emergency surgery due to persistent bleeding into the airway and airway obstruction during follow-up. Postoperative pneumonia and atelectasis could be prevented by manual removal of the residual hematoma.

Giant Cell Granuloma in a Child: Case Report

2007 ◽  
Vol 31 (4) ◽  
pp. 257-259
Author(s):  
Mariana Passos ◽  
Rebeca Azevedo ◽  
Maria Eliza Janini ◽  
Lucianne Cople Maia
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Giant Cell ◽  
Histopathological Examination ◽  
Posterior Region ◽  
Giant Cell Granuloma ◽  
Total Removal ◽  
Central Giant Cell Granuloma ◽  
The Right

This article describes a case of central giant cell granuloma in the right posterior region of mandible in a 10- year-old girl. The lesion was removed by curettage and a histopathological examination was carried out. Clinical and radiographic follow-up showed total removal of the lesion. The importance of early diagnosis of this type of lesion is emphasized, mainly in children.

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