scholarly journals UNE LOCALISATION RARE DUN SCHWANNOME ORBITAIRE A RARE LOCALIZATION OF AN ORBITAL SCHWANNOMA

2020 ◽  
Vol 8 (9) ◽  
pp. 941-944
Author(s):  
Zahra Sayad ◽  
◽  
Bouchra Dani ◽  
Malik Boulaadas
Keyword(s):  
Iliac Crest ◽  
Benign Tumor ◽  
Histological Analysis ◽  
Surgical Excision ◽  
Ocular Motility ◽  
Iliac Crest Graft ◽  
Complete Surgical Excision ◽  
Operative Specimen ◽  
Rare Benign Tumor ◽  
The Right

Introduction: The infraorbital schwannoma or neuroma is a rare benign tumor of the orbit. Its clinical and radiological presentation is not very specific. Its diagnosis is essentially histological. Observation: We report the case of a 46-year-old woman, diabetic under treatment, consulting for an irreducible, non-axial and non-pulsatile exophthalmos. Clinical examination of the left eye found visual acuity corrected to 8/10 without limitation of ocular motility or diplopia. The examination of the right eye is unremarkable.The orbital CT objectified a mass measuring 25.3mm × 13.8mm, homogeneous of the floor of the left orbit, pushing the eyeball up and out. The orbital floor was pushed inferiorly by the mass however, its integrity was preserved. Tumor excision was performed via the sub-ciliary cutaneous incision with reconstruction of the floor by an iliac crest graft. The histological analysis allowed us to have a definite diagnosis of schwannoma. Conclusion:The schwannoma is a rare tumor of the orbit. Its diagnosis is established solely by anatomopathological study of the operative specimen. Its treatment is based on a complete surgical excision to avoid any recurrence.

Soft-Tissue Chondroma in the Right Hallux: A Case Report

2019 ◽  
Vol 109 (6) ◽  
pp. 451-454
Author(s):  
Xingpei Hao ◽  
Joon Yim ◽  
Chenfeng Qi ◽  
Gene Mirkin
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Physical Examination ◽  
Benign Tumor ◽  
Proximal Phalanx ◽  
Surgical Excision ◽  
Cartilaginous Matrix ◽  
Rare Benign Tumor ◽  
The Right ◽  
Hands And Feet

Soft-tissue chondroma is a rare, benign tumor. It is predominantly found in the hands and feet, but rarely in the toes. In this article, we report a digital soft-tissue chondroma that presented as a painful nodule of 5 years' duration in a 67-year-old man. Physical examination revealed a round, solid, movable nodule measuring 7 mm in diameter. Radiographs showed faint linear calcifications in the nodule under the right hallux proximal phalanx neck. The mass was completely excised, and pathologic observation revealed a mass composed of mature chondrocytes in a cartilaginous matrix, consistent with a chondroma. Even though this is a benign tumor, it needs to be differentiated from other tumors, including schwannoma, leiomyoma, chondrosarcoma, and others. Surgical excision is the preferred treatment.

scholarly journals Primary extradural ectopic orbital Meningioma.

2021 ◽  
pp. 10-12
Keyword(s):  
Visual Impairment ◽  
Recurrence Rate ◽  
Benign Tumor ◽  
Surgical Excision ◽  
Good Prognosis ◽  
Complete Surgical Excision ◽  
Rare Benign Tumor ◽  
Long Time ◽  
Diagnostic Difficulties ◽  
Orbital Meningioma

Orbital meningioma is a rare benign tumor. However, the existence of ectopic orbital meningiomas was debated for long time and this lesion might be underreported. Complete surgical excision could achieve a good prognosis without visual impairment. The recurrence rate is still considerable. The aim of this report was to highlight the diagnostic difficulties and management characteristics.

scholarly journals Primary Tracheal Papilloma: A Case Report

2020 ◽  
Vol 49 (2) ◽  
pp. 44-47
Author(s):  
Md Hasanul Haque ◽  
Belayat Hossain Siddique ◽  
Abirvab Naha ◽  
Abdus Sattar ◽  
Nigar Sultana ◽  
...  
Keyword(s):  
Surgical Excision ◽  
Current Standard ◽  
Epithelial Tumor ◽  
Delayed Treatment ◽  
Complete Surgical Excision ◽  
Current Standard Treatment ◽  
Squamous Cell Papilloma ◽  
The Right ◽  
Specific Symptoms ◽  
Histopathological Result

Solitary papilloma in the respiratory tract is a rare benign epithelial tumor which is complete surgical excision of the current standard treatment for this type of tumor. Here a case of solitary tracheal papilloma treated by surgical resection is reported. Due to rarity and non-specific symptoms, tracheal papilloma always subjected to misdiagnosed and suffer from delayed treatment. In this case, a forty two years male has been presented with a recurrent non-productive irritative cough, a progressive shortness of breath, expiratory stridor and occasional hemoptysis. The patient was previously diagnosed as a case of bronchial asthma by a Pulmonologist and wrongly treated as well. CT scan revealed an intraluminal tracheal mass arises from the right side of the tracheal wall opposite c6-c7 vertebrae. The tumour was removed by endoscopic excision. The histopathological result confirms the diagnosis of squamous cell papilloma. No complications occur during surgery and no recurrence was observed in six months after surgery on followup. Bangladesh Med J. 2020 May; 49(2) : 44-47

Eccrine Syringofibroadenoma of the Heel

2016 ◽  
Vol 106 (1) ◽  
pp. 76-78
Author(s):  
Nathalia Doobay ◽  
Jason Mallette
Keyword(s):  
Benign Tumor ◽  
Surgical Excision ◽  
Foot Pain ◽  
Rare Benign Tumor ◽  
Ductal Differentiation

Eccrine syringofibroadenoma is a rare, benign tumor of eccrine ductal differentiation, typically presenting in the extremities. Herein we report a case of a 77-year-old man with pain in the lateral midfoot and the presence of an eccrine syringofibroadenoma lesion in the lateral heel. On surgical excision of the lesion, the foot pain promptly resolved, and at the most recent follow-up visit, the patient remained pain free.

Inflammatory myofibroblastic tumour of the conjunctiva masquerading as ocular surface squamous neoplasia

2020 ◽  
pp. 112067212097361
Author(s):  
Manpreet Singh ◽  
Manu Saini ◽  
Debajyoti Chatterjee ◽  
Aditi Mehta ◽  
Manpreet Kaur ◽  
...  
Keyword(s):  
Amniotic Membrane ◽  
Ocular Surface ◽  
Surgical Excision ◽  
Excision Biopsy ◽  
Inflammatory Myofibroblastic Tumour ◽  
Complete Surgical Excision ◽  
Oral Steroids ◽  
Rare Site ◽  
The Right

A 63-year-male had painless, progressive, yellowish-pink, immobile conjunctival mass with prominent feeder vessels in the right eye of 1-year duration. The rest of the ophthalmic examination was unremarkable. MRI showed no extension into orbit or extraocular muscles. An excision biopsy with the amniotic membrane patch was performed. Histopathology confirmed inflammatory myofibroblastic tumour (IMT) with SMA and calponin positivity on immunohistochemistry. Complete surgical excision, amniotic membrane, and oral steroids provided long-term relief from recurrence. The conjunctiva is a rare site for IMT, and IMT should be kept in the differentials for atypical cases of ocular surface neoplasia.

Pelvic Schwannoma: Robotic Laparoscopic Resection

2012 ◽  
Vol 72 (1) ◽  
pp. ons2-ons5 ◽  
Author(s):  
Constance Deboudt ◽  
Jean-Jacques Labat ◽  
Thibault Riant ◽  
Olivier Bouchot ◽  
Roger Robert ◽  
...  
Keyword(s):  
Peripheral Nerves ◽  
Benign Tumor ◽  
Laparoscopic Resection ◽  
Resonance Imaging ◽  
Pelvic Nerve ◽  
Neurological Sequelae ◽  
Nerve Sheath ◽  
Rare Benign Tumor ◽  
The Right

Abstract Background: Schwannoma is a rare benign tumor of peripheral nerves arising from Schwann cells of the ubiquitous nerve sheath. Objective: To describe the operative steps and technical aspects of robotic laparoscopic resection of pelvic schwannoma. Methods: We describe 2 patients with pelvic schwannoma: a 34-year-old woman with schwannoma of the right lumbosacral trunk and a 58-year-old woman with schwannoma of a left S1 nerve. Pain was the main symptom in both patients. The diagnosis was confirmed by magnetic resonance imaging and nerve biopsies. Both patients were operated on by robotic laparoscopy. Results: Lesions were totally enucleated after incising the epineurium. After dissection of the schwannoma, the vascular pedicle and nerve fascicles involved were identified, coagulated, and then sectioned. The remaining fascicles of the nerve were preserved. The postoperative course was uneventful in both patients. With follow-up of 9 and 13 months, both patients obtained complete pain relief with no neurological sequelae. Conclusion: Robotic laparoscopic resection of pelvic nerve tumors such as schwannomas is technically feasible.

scholarly journals Spinal osteoid osteoma: Surgical resection and review of literature

2020 ◽  
Vol 11 ◽  
pp. 308
Author(s):  
Abhinandan Reddy Mallepally ◽  
Rajat Mahajan ◽  
Sandesh Pacha ◽  
Tarush Rustagi ◽  
Nandan Marathe ◽  
...  
Keyword(s):  
Surgical Resection ◽  
Osteoid Osteoma ◽  
Surgical Excision ◽  
Presenting Symptoms ◽  
Complete Surgical Excision ◽  
Rare Benign Tumor ◽  
The Common ◽  
Optimal Approach ◽  
Posterior Elements

Background: Osteoid osteoma (OO) is a rare benign tumor of the spine that involves the posterior elements with 75% tumors involving the neural arch. The common presenting symptoms include back pain, deformity like scoliosis, and rarely radiculopathy. Methods: From 2011 to 2017, we evaluated cases of OO managed by posterior surgical resection while also reviewing the appropriate literature. Results: We assessed five patients (three males and two females) averaging 36.60 years of age diagnosed with spinal OOs. Two involved the lumbar posterior elements, two were thoracic, and one was in the C3 lateral mass. All patients underwent histopathological confirmation of OO. They were managed by posterior surgical resection with/without stabilization. No lesions recurred over the minimum follow-up period of 24 months. Conclusion: Surgical excision is the optimal treatment modality for treating spinal OOs. The five patients in this study demonstrated good functional outcomes without recurrences. Further, the literature confirms that the optimal approach to these tumors is complete surgical excision with/without radiofrequency ablation.

scholarly journals Odontogenic Myxoma of the Maxilla - A Case Report

2019 ◽  
Vol 6 ◽  
Author(s):  
Adil Eabdenbtsen ◽  
Mohammed Mouzouri ◽  
Ahlam Bellouchi ◽  
Noureddine Oulali ◽  
Mohammed Bouziane ◽  
...  
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Benign Tumor ◽  
High Rate ◽  
Odontogenic Myxoma ◽  
Radical Treatment ◽  
Rare Benign Tumor ◽  
The Right

Introduction : The odontogenic myxoma is a rare benign tumor of the maxilla, whose clinical and radiological manifestations are variable and nonspecific and can be confused with other radiolucent lesions. Its origin would be the embryonic mesenchyme of the dental follicle.Case report : We report the case of odontogenic myxoma of the right maxilla, discovered by chance in a 25 year old patient. Clinically, the patient had painless, firm on palpation, swelling of the right maxilla, impeding chewing and speech. Facial CT-scan showed an expansive osteolytic process blowing the right maxilla off. A biopsy was in favor of an odontogenic myxoma. The diagnosis was based on clinical, radiological and especially anatomopathological arguments.Conclusion : The local aggressiveness of the odontogenic myxoma and its high rate of recurrence justify a radical treatment beyond the lesion’s boundaries and thus imply a postoperative repair.

scholarly journals Pigmented Paraaxillary Located "Complex" Basal Cell Carcinoma Imitating clinically irritated Melanocytic Lesion - Succesfull Surgical Approach in Bulgarian Patient

2017 ◽  
Vol 5 (4) ◽  
pp. 497-500
Author(s):  
Cristiana Voicu ◽  
Mara Mihai ◽  
Mihai Lupu ◽  
James W. Patterson ◽  
Nely Koleva ◽  
...  
Keyword(s):  
Basal Cell Carcinoma ◽  
Cell Carcinoma ◽  
Basal Cell ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Melanocytic Lesion ◽  
Complete Surgical Excision ◽  
Axillary Region ◽  
The Right ◽  
Clinical Subtype

BACKGROUND: Basal cell carcinoma (BCC) is the most frequently encountered neoplasm worldwide. While nodular BCC is the most frequent clinical subtype, other forms of BCC, such as superficial, cystic, morpheiform, infiltrative, and pigmented may also be encountered.CASE PRESENTATION: We present the case of a 67-year-old male with a relatively well-defined infiltrative, pigmented plaque with multiple colours and peripheral growth situated in the right axillary region. The histopathologic examination performed after complete surgical excision of the tumour revealed a complex pigmented BCC with macronodular, fibroepithelioma-like, cystic, focally infiltrative and basosquamous features.CONCLUSION: Uncommon locations of BCCs in sun-protected areas such as the axillary region require a higher degree of suspicion for diagnosis. The complex histology of the presented case, including subtypes with differing biologic attributes, emphasises the importance of histopathological examination in the diagnosis and therapeutic management of BCC.

scholarly journals Lymphangiofibrolipomatous hamartomaous polyp of tonsil

2019 ◽  
Vol 12 (8) ◽  
pp. e230030
Author(s):  
Sejal Mehta ◽  
Shilpy Jha ◽  
Amit Kumar Adhya ◽  
Suvradeep Mitra
Keyword(s):  
Foreign Body ◽  
Benign Tumor ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Disease Recurrence ◽  
Foreign Body Sensation ◽  
Normal Tissues ◽  
Complete Surgical Excision ◽  
Body Sensation ◽  
Benign Tumours

Benign tumours of the tonsils are rare. Majority of these lesions are diagnosed as squamous papilloma. Hamartoma is a benign tumor-like malformation. Hamartoma in tonsils is unique and only a few anecdotal cases are reported until now. Tonsillar hamartoma usually presents as unilateral or bilateral polyp with clinical features of dysphagia or foreign body sensation. Histopathologically, normal tissues are noted in a haphazard or disorganised way. We hereby present a case of 31-year-old male patient with tonsillar hamartomatous polyp presenting with the symptom of a foreign body sensation in the throat. The diagnosis of this entity and its distinction from other clinico-pathological mimickers require histopathological examination and awareness. A complete surgical excision is curative without any evidence of disease recurrence.

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