scholarly journals Temporal insular glioma–rare case report for a venous air embolism

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Swati Jain ◽  
Dinesh Kumar ◽  
Nikhilesh Chandra ◽  
Mahak Kakkar
Keyword(s):  
Rare Case ◽  
Young Male ◽  
Insular Cortex ◽  
Air Embolism ◽  
Case Presentation ◽  
Venous Air Embolism ◽  
Untoward Event ◽  
Rare Case Report ◽  
Deep Area ◽  
Rapid Presentation

Abstract Background Venous air embolism (VAE) is a well-known entity in the field of neuroanesthesia, with established surgeries and positions where its occurrence is high. The insular cortex is a deep area within the lateral sulcus, and surgeries in this area are not reported to develop VAE. Case presentation A young male being operated on the insular cortex developed VAE, had cardiac arrest, was revived, and was extubated with no residual deficit due to the untoward event. Conclusions An anesthesiologist should always be prepared for this complication due to its rapid presentation and fatal consequences.

scholarly journals Large-extension osteosarcoma with involvement of multiple maxillofacial structures: a rare case report

2020 ◽  
Vol 9 (10) ◽  
pp. e1519108461
Author(s):  
Rani Iani Costa Gonçalo ◽  
Cristiane Kalinne Santos Medeiros ◽  
Humberto Pereira Chaves Neto ◽  
Janaina Lessa de Moraes dos Santos ◽  
Adriano Rocha Germano ◽  
...  
Keyword(s):  
Rare Case ◽  
Correct Diagnosis ◽  
Malignant Neoplasm ◽  
Neck Region ◽  
Primary Treatment ◽  
Histopathological Diagnosis ◽  
Anatomical Structures ◽  
Case Presentation ◽  
Head And Neck Region ◽  
Rare Case Report

Background: Osteosarcoma is a malignant neoplasm that occurs most often in long bones, with the head and neck region being rarely affected, accounting for less than 1% of all cancers in this region. Objective: To report a rare case of a large-extension osteosarcoma with emphasis on its clinical and diagnostic aspects. Case presentation: A 43-year-old woman presenting an intraoral exophytic lesion with involvement of other maxillofacial structures, such as nostril, zygoma and orbit. Despite the initial clinical diagnosis of actinomycosis, an incisional biopsy confirmed the histopathological diagnosis of osteosarcoma, showing a wide morphological variety. Conclusion: This case highlights the importance of clinical and histopathological findings for the correct diagnosis of osteosarcoma. Moreover, it shows that, although surgical resection is the primary treatment for this neoplasia, depending on the extent of the tumor and its proximity to vital anatomical structures, the most appropriate conduct is not always feasible.

scholarly journals Extensive eye-oral-bronchial mucosal nodules with eosinopgillia: a rare case report and literature review

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Lujin Wu ◽  
Qianru Leng ◽  
Yan Wang ◽  
Daowen Wang ◽  
Danlei Yang
Keyword(s):  
Biopsy Specimen ◽  
Rare Case ◽  
Unknown Origin ◽  
Neoplastic Disease ◽  
Multisystem Disease ◽  
Case Presentation ◽  
Large Numbers ◽  
Detailed Medical History ◽  
Mucous Membranes ◽  
Rare Case Report

Abstract Background Mucosal nodules can be caused by infection, inflammation and neoplastic disease. Many noninfectious diseases, such as eosinophilia, amyloidosis, sarcoidosis, Wegener’s granuloma, langerhans cell histiocytosis etc., are associated with the formation of multisytem mucosal nodules, especially significant bronchial lesions. Detailed medical history, comprehensive metabolic profile, biopsy specimen and imaging examinations are required for differentiating among these disorders. The process of diagnosis and treatment of our patient’s mucosal nodules was challenging, which could be helpful to similar cases. Case presentation We represent a case of a 29-year-old woman with plentiful nodules of unknown origin on extensive mucous membranes. Biopsy specimen reports inflammatory lesions with large numbers of neutrophils, lymphocytes, and varying degrees of eosinophils. Treatment of anti-infection, anti-tussive and anti-allergic was ineffective, but glucocorticoid showed great improvement to her symptoms. Conclusion We experienced a rare case with plentiful nodules of unknown origin on extensive mucous membranes. She may be a specific phenotype of eosinophilia or may be a novel multisystem disease with respiratory system as the primary symptom. The diagnosis of our patient remains unclear, but tentative glucocorticoid therapy was beneficial.

scholarly journals Lipoma in Penis : A Rare Case Report

2013 ◽  
Vol 3 (1) ◽  
pp. 24-25
Author(s):  
T Ahmed ◽  
MA Kalam ◽  
II Mannan ◽  
MA Simi
Keyword(s):  
Case Report ◽  
Plastic Surgery ◽  
Male Patient ◽  
Rare Case ◽  
Young Male ◽  
Histopathological Analysis ◽  
Review Of The Literature ◽  
Ventral Aspect ◽  
Rare Case Report ◽  
Pedunculated Tumor

In this article we report one case of lipoma of the penis in a twenty three years old young male. This site of lipoma is rare. A case of a young male patient who consulted for removal of a penile lump is presented. The small, regular, wellcircumscribed pedunculated tumor localized on the ventral aspect of the penis was excised. The histopathological analysis showed a benign lipoma. A review of the literature showed lipoma of the penis to be very uncommon. For this reason, we were prompted to report this case.DOI: http://dx.doi.org/10.3329/bdjps.v3i1.15003 Bangladesh Journal of Plastic Surgery 2012, 3(1): 24-25

Unique Coexistence of Severe Primary Pulmonary Hypertension and Marfanoid Habitus in a Young Male - An Interesting and Rare Case Report

CHEST Journal ◽  
2014 ◽  
Vol 145 (3) ◽  
pp. 64A
Author(s):  
Ram K. Chopra ◽  
Sanesh Garde ◽  
Chintan Patel ◽  
Dhiraj Jain ◽  
Omkar Kajale ◽  
...  
Keyword(s):  
Pulmonary Hypertension ◽  
Case Report ◽  
Rare Case ◽  
Primary Pulmonary Hypertension ◽  
Young Male ◽  
Rare Case Report

scholarly journals Clear Cell Primary Seminal Vesicle Carcinoma in a Young Male-A Rare Case Report

2018 ◽  
Author(s):  
Saurabh Gaur ◽  
Sunil B Pillai ◽  
Padmaraj Hegde ◽  
Arun Kumar Chawla ◽  
Aseem Kapadia
Keyword(s):  
Case Report ◽  
Seminal Vesicle ◽  
Rare Case ◽  
Clear Cell ◽  
Young Male ◽  
Rare Case Report

scholarly journals Buerger’s disease in female: rare case report

2018 ◽  
Vol 5 (4) ◽  
pp. 1571
Author(s):  
Abhijit A. Bhoyate ◽  
Lekshmi Priya R. ◽  
Vidyanand Tripathi ◽  
Piyushkumar Agrawal ◽  
G. S. Moirangthem
Keyword(s):  
Case Report ◽  
Vascular Disease ◽  
Rare Case ◽  
Young Male ◽  
Thromboangiitis Obliterans ◽  
Buerger’S Disease ◽  
Buerger's Disease ◽  
Rare Case Report ◽  
Arteries And Veins

Thromboangiitis obliterans (Bureger’s disease) is a vascular disease characterized by a segmental, non-atherosclerotic inflammation of the small and medium-sized arteries and veins of the distal extremities mostly affecting young male smokers and rarely females. Only a few cases with histologic proof of the disease in females have ever been recorded in literature. We report a rare case of Buerger’s disease in a 55 years old female.

scholarly journals Scrotal chondroma in a young male: A rare case report

2016 ◽  
Vol 59 (2) ◽  
pp. 238 ◽  
Author(s):  
Brijesh Thakur ◽  
Sanjeev Kishore ◽  
Sheenam Azad ◽  
Sandip Kudesia
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Young Male ◽  
Rare Case Report
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