A Frontal Retrobulbar Mucocele with Lytic Lesion at Orbital Plate and Orbital Ridge, Rare Case Report

Mucoceles can occurs when there is obstruction of drainage passage of mucosa of paranasal sinus. Some time it can cause pressure at eye ball and can cause proptosis. A old man admitted at Bangabandhu Sheikh Mujib Medical University with the complaints of right orbital swelling with proptosis of right eye ball. Also complaints of progressive visual bluring & headache for some time. The mucocele was operated by frontal craniotomy and excised completely. As this is a ran case and so few an reported. Bangladesh Journal of Neuroscience 2011; Vol. 27 (2) : 105-107 DOI: http://dx.doi.org/10.3329/bjn.v27i2.17578

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Paranasal sinus mucormycosis in an immunocompetent host: A rare case report

Journal of Oral and Maxillofacial Surgery Medicine and Pathology ◽

10.1016/j.ajoms.2011.09.002 ◽

2012 ◽

Vol 24 (2) ◽

pp. 106-109 ◽

Cited By ~ 1

Author(s):

Amit Mohan ◽

Deepak Pai ◽

Shalini Krishnan

Keyword(s):

Case Report ◽

Paranasal Sinus ◽

Rare Case ◽

Immunocompetent Host ◽

Rare Case Report

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Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report

Clinical Rhinology An International Journal ◽

10.5005/jp-journals-10013-1249 ◽

2015 ◽

Vol 8 (3) ◽

pp. 124-126

Author(s):

Ankita Joshi ◽

Chinmay Sundarray ◽

Krishna Arpita Sahoo

Keyword(s):

Case Report ◽

Paranasal Sinus ◽

Paranasal Sinuses ◽

Rare Case ◽

The Other ◽

High Rate ◽

Unknown Etiology ◽

Structural Variations ◽

The Third ◽

Rare Case Report

ABSTRACT Paranasal sinus anatomical anomalies with unknown etiology are common. Paranasal sinus-related diseases are associated with so high rate of morbidities, it becomes essential to identify the structure and pathophysiology of the paranasal sinuses. Computed tomography (CT) is a valuable tool in displaying its anatomy, any anatomic variations and diseases. As paranasal sinus development is a complex and long-lasting process, there are great structural variations between individuals. Maxillary and/or frontal sinus aplasia or hypoplasia are more common than the other types. Several degrees and combinations of aplasias and hypoplasias have been reported; however, there is only two case of total paranasal sinus aplasia in the literature. Here, we present the third case of total paranasal sinus aplasia, and the first ever case reported from India. How to cite this article Joshi A, Sundarray C, Sahoo KA. Bilateral Total Aplasia of Paranasal Sinuses: A Rare Case Report. Clin Rhinol An Int J 2015;8(3):124-126.

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Extramedullary plasmacytoma of Paranasal sinus: A rare case report

IP Journal of Otorhinolaryngology and Allied Science ◽

10.18231/j.ijoas.2020.007 ◽

2020 ◽

Vol 3 (1) ◽

pp. 29-31

Author(s):

Harendra Kumar Gautam ◽

◽

Shalini Tripathi ◽

Keyword(s):

Case Report ◽

Paranasal Sinus ◽

Rare Case ◽

Extramedullary Plasmacytoma ◽

Rare Case Report

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Foramen Magnum Meningioma: A Rare Case Report

Chattagram Maa-O-Shishu Hospital Medical College Journal ◽

10.3329/cmoshmcj.v13i3.21031 ◽

2014 ◽

Vol 13 (3) ◽

pp. 69-73

Author(s):

Haradhan Deb Nath ◽

Kanak Kanti Barua ◽

Shahnewaj Bari ◽

Hafizul Amin

Keyword(s):

Case Report ◽

Vertebral Artery ◽

Rare Case ◽

Cranial Nerves ◽

Foramen Magnum ◽

Rare Case Report ◽

Proper Training ◽

Lower Cranial Nerves ◽

Medical University

Background: Foramen magnum meningiomas are challenging tumors, requiring special considerations because of the vicinity of the medulla oblongata, the lower cranial nerves, and the vertebral artery. After detailing the relevant anatomy of the foramen magnum area, we will explain our classification system based on the compartment of development, the dural insertion, and the relation to the vertebral artery. Method: A 35 years age lady with foramen magnum meningioma was operated at the Department of Neurosurgery, Bangabandhu Sheikh Mujib Medical University 6 months back. A case report was taken before surgery and 6 month follow up was done after operation. Conclusion: As foramen magnum meningioma is very difficult to approach, with the help of microscope with proper training. We can remove completely without any deficit.DOI: http://dx.doi.org/10.3329/cmoshmcj.v13i3.21031

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Case of tuberculosis acromioclavicular joint presenting as lytic lesion in lateral end clavicle: rare case report

International Journal of Orthopaedics Sciences ◽

10.22271/ortho.2015.v1.i3.04 ◽

2015 ◽

Vol 1 (3) ◽

pp. 17-17

Author(s):

Praveen Kumar Pandey ◽

◽

Inder Pawar ◽

Raaghav Rai Verma ◽

◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Acromioclavicular Joint ◽

Lytic Lesion ◽

Rare Case Report

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Oral Surgery Procedures in a Patient with Hajdu-Cheney Syndrome Treated with Denosumab—A Rare Case Report

International Journal of Environmental Research and Public Health ◽

10.3390/ijerph18179099 ◽

2021 ◽

Vol 18 (17) ◽

pp. 9099

Author(s):

Magdalena Kaczoruk-Wieremczuk ◽

Paulina Adamska ◽

Łukasz Jan Adamski ◽

Piotr Wychowański ◽

Barbara Alicja Jereczek-Fossa ◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Alveolar Bone ◽

Oral Surgery ◽

Nuclear Factor Κb ◽

Osteonecrosis Of The Jaw ◽

Prosthetic Reconstruction ◽

Dental Procedures ◽

Rare Case Report ◽

Medical University

Background: Hajdu-Cheney syndrome (HCS) is a very rare autosomal-dominant congenital disease associated with mutations in the NOTCH2 gene. This disorder affects the connective tissue and is characterized by severe bone resorption. Hajdu-Cheney syndrome most frequently affects the head and feet bones (acroosteolysis). Case report: We present an extremely rare case of a 34-year-old male with Hajdu-Cheney syndrome. The patient was admitted to the Department of Oral Surgery, Medical University of Gdańsk, in order to perform the extraction of three teeth. These teeth were not eligible for conservative treatment and prosthetic reconstruction. The patient was treated with denosumab (angiogenesis and receptor activator of nuclear factor-κB RANK ligand inhibitor, RANKL). Discussion: Denosumab is a monoclonal antibody against RANKL. This drug works through a suppression of osteoclast activity. In cases of patients in which the pathway of the RANK/RANKL/osteoprotegerin is dysregulated, denosumab has been approved for the treatment off-label. In patients receiving denosumab, a delayed wound healing in the oral cavity and osteonecrosis may occur. Dental procedures involving the alveolar bone process (tooth extractions and bone alveoloplasty) may be a risk factor for medication-related osteonecrosis of the jaw (MRONJ). Spontaneous osteonecrosis is rarely observed. MRONJ consists of the destruction of exposed bone, with the exposure persisting for a minimum of 6–8 weeks. This is the first article about an HCS patient treated with denosumab who underwent invasive oral surgery procedures. This case report highlights the difficulties for professionals occurring during the oral surgery procedures in such patients.

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