scholarly journals Clinical Observations in Nasal and Paranasal Sinus Mycosis; A Case Report.

1999 ◽  
Vol 92 (2) ◽  
pp. 151-155
Author(s):  
Hideaki KITA ◽  
Kohji ASAKURA ◽  
Tadataka ISHIKAWA ◽  
Tetsuo HIMI ◽  
Yasuaki HARABUCHI ◽  
...  
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Clinical Observations

Epidermoid brain cysts: a case report and a literature review

2021 ◽  
pp. 358-371
Author(s):  
Maksim Vladimirovich Shpagin ◽  
Anton Viktorovich Yarikov ◽  
Denis Nikolaevich Nikitin ◽  
Igor Anatolievich Lobanov ◽  
Ivan Aleksandrovich Laganin ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Cerebellopontine Angle ◽  
Clinical Manifestations ◽  
Complex Treatment ◽  
Brain Pathology ◽  
Epidermoid Cysts ◽  
Histological Picture ◽  
Clinical Observations ◽  
Brain Cysts

The article is devoted to rare brain pathology, i.e. epidermoid cysts. The histological picture of the tumor is described; the classification is given. On the basis of our own clinical observations and a literature review, the features of the clinical manifestations of cholesteatoma of the cerebellopontine angle, modern approaches to the diagnosis and tactics of complex treatment are presented.

scholarly journals A Huge Cemento-Ossifying Fibroma of Paranasal Sinus: A Case Report

2012 ◽  
Vol 55 (3) ◽  
pp. 146-149
Author(s):  
Ibrahim Erdim ◽  
Zahide Mine Yazici ◽  
Rasim Yilmazer ◽  
Nurten Sever ◽  
Fatma Tulin Kayhan
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Male Patient ◽  
Paranasal Sinuses ◽  
Surgical Excision ◽  
Ossifying Fibroma ◽  
Radiological Appearance ◽  
Close Observation ◽  
Slow Growing

Cemento-ossifying fibroma is a well-bordered, slow-growing, benign fibro-osseous disease. Although its localization is generally in the mandible, it can be seen in any area of the craniofacial region. Radiology and histopathology help to diagnose the condition. Treatment is based on close observation and/or surgical excision. In this case, we report the case of a 62-year-old male patient who had a large radiological appearance, cemento-ossifying fibroma in the paranasal sinuses.

Pneumosinus dilatans, pneumocoele or air cyst? A case report and literature review

2011 ◽  
Vol 126 (1) ◽  
pp. 88-93 ◽  
Author(s):  
B M Teh ◽  
C Hall ◽  
S W Chan
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Maxillary Sinus ◽  
Key Words ◽  
Paranasal Sinus ◽  
Facial Pain ◽  
Surgical Intervention ◽  
Pneumosinus Dilatans

AbstractBackground:Pathological paranasal sinus expansion secondary to air is uncommon. However, this condition may be symptomatic or cosmetically apparent, requiring surgical intervention. Various terms have been used to describe this condition, and nomenclature is controversial.Method:An 18-year-old man presented with right facial pain, and was subsequently found to have pneumosinus dilatans of the maxillary sinus. A search was conducted of the PubMed, Medline and Embase databases, using the key words ‘pneumosinus dilatans’, ‘pneumoc(o)ele’, ‘pneumatoc(o)ele’ and ‘maxillary sinus’. Articles were also hand-searched. Relevant articles published in English were reviewed.Results:The literature review identified 36 cases involving the maxillary sinus (including the present case), with 19 cases reported as pneumosinus dilatans, 12 as pneumocoeles, two as pneumatocoeles, two as pneumosinus dilatans multiplex and one as an air cyst. However, based on the strict classification described by Urken et al., the majority of these cases should be reclassified as pneumocoeles.Conclusion:Whilst the nomenclature of this pathology is confusing, distinctions of terminology do not alter the management. Hence, we support the use of the term ‘air cyst’, to incorporate all these lesions.

scholarly journals A Case Report of a Solitary Fibrous Tumor Occurring in the Paranasal Sinus

2007 ◽  
Vol 100 (8) ◽  
pp. 669-674 ◽  
Author(s):  
Masaki Kawabata ◽  
Shoji Matsune ◽  
Yuichi Kurono
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Solitary Fibrous Tumor ◽  
Fibrous Tumor

Endoscopic removal of paranasal sinus osteoma: A case report

2002 ◽  
Vol 60 (2) ◽  
pp. 230-232 ◽  
Author(s):  
Halit Akmansu ◽  
Adil Eryilmaz ◽  
Muharrem Dagli ◽  
Hakan Korkmaz
Keyword(s):  
Case Report ◽  
Paranasal Sinus ◽  
Endoscopic Removal

Meningioma of the paranasal sinus: A case report

2007 ◽  
Vol 34 (3) ◽  
pp. 397-400 ◽  
Author(s):  
Kazuyuki Kainuma ◽  
Yutaka Takumi ◽  
Takeshi Uehara ◽  
Shin-ichi Usami
Keyword(s):  
Case Report ◽  
Paranasal Sinus

scholarly journals Metastatic Renal Cell Carcinoma in a Paranasal Sinus; A Case Report.

1993 ◽  
Vol 86 (6) ◽  
pp. 829-833
Author(s):  
Akira Kodama ◽  
Kazutomo Kitajima ◽  
Ken-ichi Kataoka ◽  
Yutaka Nakaishi
Keyword(s):  
Renal Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Paranasal Sinus ◽  
Metastatic Renal Cell Carcinoma ◽  
Renal Cell

scholarly journals PEUTZ–JEGHERS–TOURAINE' SYNDROME (CASE REPORT)

2018 ◽  
Vol 5 (3) ◽  
pp. 121-125
Author(s):  
F. Nishanov ◽  
B. Abdullajanov ◽  
N. Bozorov ◽  
M. Nishanov ◽  
F. Hamidov ◽  
...  
Keyword(s):  
Small Intestine ◽  
Case Report ◽  
Surgical Treatment ◽  
Abdominal Surgery ◽  
Intestinal Obstruction ◽  
Emergency Surgery ◽  
Multiple Polyposis ◽  
Clinical Observations ◽  
Colonic Bleeding

PEUTS-JEGHERS TOURINE SYNDROMENishanov F., Abdullajanov B., Bozorov N.,Nishanov М., Hamidov F., Mishenina E.Authoris present two clinical observations syndrome Peutz-Jeghers Touraine, wich is hereditary and appears periorifitsial lentiginosis multiple polyposis of the small intestine (jejunum mainly)and it complications such as intestinal obstruction invaginated which combines intra colonic bleeding. The authors concluded that abdominal surgery should know and remember about the syndromePeutz-Jeghers Touraine,in order to avoid diagnostic and tactical errors and promptly provide expert surgical treatment for the.Key words: syndrome, emergency surgery, perioficial lentinginosis, invagination intestinal obstruction. РезюмеСИНДРОМ ПЕЙТЦА-ЕГЕРСА-ТУРЕНАНішанов Ф., Абдуллажанов Б., Бозоров Н.,Нішанов М., Хамідов Ф., Мішеніна Е. Автори наводять два клінічних спостереження синдрому Пейтца-Егерса-Турена, який має спадковий характер і проявляється періоріфіціальним лентігінозом, множинним поліпозом тонкої кишки (переважно порожньої) і його ускладнень у вигляді інвагінаційної кишкової непрохідності, яка поєднується з внутрішньокишковою кровотечею. Автори роблять висновок,що абдомінальним хірургам слід знати і пам'ятати про синдром Пейтца - Егерса - Турена, що дозволить уникнути діагностичних і тактичних помилок і своєчасно надати кваліфіковану екстрену хірургічну допомогу.Ключові слова: синдром, екстрена хірургія, періоріфіціальнийлентігіноз, інвагінаційна кишкова непрохідність. РезюмеСИНДРОМ ПЕЙТЦА-ЕГЕРСА-ТУРЕНАНишанов Ф., Абдуллажанов Б., Бозоров Н., Нишанов М., Хамидов Ф., Мишенина Е.Авторы приводят два клинических наблюдения синдрома Пейтца-Егерса-Турена, который имеет наследственный характер и проявляется периорифициальным лентигинозом, множественным полипозом тонкой кишки (преимущественно тощей) и его осложнений в виде инвагинационной кишечной непроходимости, которая сочетается внутрикишечным кровотечением. Авторы заключают что, абдоминальным хирургам следует знать и помнить о синдроме Пейтца – Егерса - Турена, что позволит избежать диагностических и тактических ошибок и своевременно оказать квалифицированную экстренную хирургическую помощь. Ключевые слова: синдром, экстренная хирургия, периорифициальный лентигиноз, инвагинационной кишечной непроходимости. 

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