1.Proptosis from a cephalhematoma in a twelve-year-old girl: a case report.
Kyeong Seok LEE ; Won Kyeong BAE ; Heung Sun LEE ; Hack Gun BAE ; Il Gyu YUN
Journal of Korean Medical Science 1991;6(3):251-254
We report a unique case of a 12-year-old girl with unilateral proptosis form orbital extension of an extensive bilateral cephalhematoma. Loss of vision in the left eye due to severe proptosis was reversed by prompt aspiration and tarsorrhaphy.
Cerebral Hemorrhage/*complications/radiography
;
Child
;
Exophthalmos/*etiology/radiography
;
Female
;
Hematoma/*complications/radiography
;
Humans
2.Weber-Christian disease presenting with proptosis: a case report.
Sang Hoon HYUN ; Young Mo KANG ; Chan Duck KIM ; Jong Myung LEE ; In Taek KIM ; Nung Soo KIM
Journal of Korean Medical Science 2000;15(2):247-250
Weber-Christian disease (WCD) is a rare inflammatory disease of adipose tissue, which is characterized by painful cutaneous nodules and constitutional symptoms. Although any area of the body containing fat can be affected by WCD, the involvement of retrobulbar fat is uncommon and proptosis is a rare presenting manifestation. We report a case who presented with proptosis of the right eye which is accompanied by painful subcutaneous nodules, high fever and myalgia. Biopsies of retrobulbar tissue and suprapubic nodule showed lobular panniculitis with mixed cellular infiltration, mainly composed of histiocytes and lymphocytes. He responded well to high-dose glucocorticoid.
Adult
;
Biopsy
;
Case Report
;
Exophthalmos/pathology*
;
Exophthalmos/etiology*
;
Exophthalmos/drug therapy
;
Glucocorticoids/administration & dosage
;
Human
;
Magnetic Resonance Imaging
;
Male
;
Panniculitis, Nodular Nonsuppurative/pathology*
;
Panniculitis, Nodular Nonsuppurative/drug therapy
;
Panniculitis, Nodular Nonsuppurative/complications*
3.Weber-Christian disease presenting with proptosis: a case report.
Sang Hoon HYUN ; Young Mo KANG ; Chan Duck KIM ; Jong Myung LEE ; In Taek KIM ; Nung Soo KIM
Journal of Korean Medical Science 2000;15(2):247-250
Weber-Christian disease (WCD) is a rare inflammatory disease of adipose tissue, which is characterized by painful cutaneous nodules and constitutional symptoms. Although any area of the body containing fat can be affected by WCD, the involvement of retrobulbar fat is uncommon and proptosis is a rare presenting manifestation. We report a case who presented with proptosis of the right eye which is accompanied by painful subcutaneous nodules, high fever and myalgia. Biopsies of retrobulbar tissue and suprapubic nodule showed lobular panniculitis with mixed cellular infiltration, mainly composed of histiocytes and lymphocytes. He responded well to high-dose glucocorticoid.
Adult
;
Biopsy
;
Case Report
;
Exophthalmos/pathology*
;
Exophthalmos/etiology*
;
Exophthalmos/drug therapy
;
Glucocorticoids/administration & dosage
;
Human
;
Magnetic Resonance Imaging
;
Male
;
Panniculitis, Nodular Nonsuppurative/pathology*
;
Panniculitis, Nodular Nonsuppurative/drug therapy
;
Panniculitis, Nodular Nonsuppurative/complications*
4.Pay attention to the causes and complications associated with surgical reconstruction of orbital fractures.
Chinese Journal of Stomatology 2011;46(8):463-466
Diplopia
;
etiology
;
Enophthalmos
;
etiology
;
Exophthalmos
;
etiology
;
Facial Nerve Injuries
;
etiology
;
Hemorrhage
;
etiology
;
Humans
;
Intraoperative Complications
;
etiology
;
prevention & control
;
Orbit
;
blood supply
;
surgery
;
Orbital Fractures
;
surgery
;
Postoperative Complications
;
etiology
;
prevention & control
;
Reconstructive Surgical Procedures
;
adverse effects
;
Reflex, Trigeminocardiac
;
Vision, Low
;
etiology
5.Therapy for Graves' ophthalmopathy.
Jianguo ZHENG ; Xia ZHANG ; Rixiang GONG ; Ji WANG ; Tianzhi TAN
Journal of Biomedical Engineering 2004;21(5):876-879
Graves' ophthalmopathy (GO) is also called thyroid-related eye disease, infiltrative ophthalmopathy, which is related with the autoimmunity of thyroid, especially hyperthyroidism. Its morbidity ragnes from five percent to ten percent of hyperthyroidism, and the morbidity of male patients is higher than that of the female patients. The treatment of severe GO is a difficult task for doctors. The therapeutic effect is not always satisfactory. In order to solve this knotty problem, researchers have been devoting themselves to the development of new therapeutic methods. Here, the development of the therapies for GO is introduced, and the trends of treatments are prospected.
Combined Modality Therapy
;
Exophthalmos
;
etiology
;
radiotherapy
;
therapy
;
Graves Disease
;
complications
;
radiotherapy
;
therapy
;
Humans
;
Immunoglobulins
;
therapeutic use
;
Prednisolone
;
therapeutic use
6.A case of proptosis by traumatic delayed meningo-encephalocele.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(11):1040-1041
A case of traumatic delayed meningo-encephalocele suffered orbital fracture, but bony defects in frontal sinus had not been found on CT scanning. We treated the patient with surgery of intranasal endoscopy and repaired the skull base defect successfully during the first attempt. There was no recurrence in 10 months followed up. The leak site may not correlate with imaging in traumatic delayed meningo-encephalocele by comparing operative findings with the imaging estimate and endoscopy. Therefore, endoscopical approaching is effective in seeking and treatment.
Encephalocele
;
complications
;
Endoscopy
;
Exophthalmos
;
etiology
;
Frontal Sinus
;
pathology
;
Humans
;
Orbital Fractures
;
pathology
;
Recurrence
;
Tomography, X-Ray Computed
7.Clinical analysis of patients with sphenoid sinus mucocele and literature review.
Xueming LIU ; Xueping WANG ; Jie WEN ; Chang LIU ; Yuxiang CAI ; Yong FENG ; Chufeng HE
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(21):1850-1852
OBJECTIVE:
Aimed to analyse the clinical features of the patients with sphenoid sinus mucocele, achieve earlier diagnosis and more timely intervention and decrease the occurrence of misdiagnoses.
METHOD:
A retrospective study was first conducted in patients with sphenoid sinus mucoele treated in Xiangya hospital from Jan 2000 to Jan 2015. Then literature reports on this disease were collected and analyzed from China National Knowledge Infrastructure (CNKI) and Wan Fang database.
RESULT:
We collected 82 patients with sphenoid sinus mucocele treated in Xiangya hospital. There were 52 patients presented with headache, 31 patients presented with visual impairment, 10 patients presented with cranial nerve palsy, 2 patients presented with exophthalmos, 15 patients presented with nasal symptoms, and 5 patients with no obvious symptoms. There was no significant difference for symptoms distribution between male and female patients (P > 0.05). Among 45 patients with headache as first symptom and 10 patients with ethmoid sinus mucocele, there were 18 patients and 8 patients subsequently suffering from visual impairment, respectively. We also collected 161 patients in literature except for enrolling, the 82 patients treated in Xiangya hospital, and found that headache was the most common symptom, followed by visual impairment, in the two independent cohorts.
CONCLUSION
To the best of our knowledge, this is the study of maximum sample for sphenoid sinus mucocele in China. Headache and visual impairment are the most common symptoms for sphenoid sinus mucocele. Surgical treatment should be early performed when the desease accompanied with headache or ethmoid sinus mucocele, to avoid other complications such as visual impairment and even blindness.
China
;
Cranial Nerve Diseases
;
etiology
;
Databases, Factual
;
Diagnostic Errors
;
Ethmoid Sinus
;
Exophthalmos
;
etiology
;
Female
;
Headache
;
etiology
;
Humans
;
Male
;
Mucocele
;
complications
;
diagnosis
;
pathology
;
Paranasal Sinus Diseases
;
Retrospective Studies
;
Sphenoid Sinus
;
pathology
;
Vision Disorders
;
etiology
8.Clinical analysis of rhinogenous ophthalmocele.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2007;21(2):69-70
OBJECTIVE:
To investigate the diagnosis and treatment of rhinogenous ophthalmocele, to reduce misdiagnosis and missed diagnosis rate.
METHOD:
Sixty-two patients with rhinogenous ophthalmocele disease in our hospital from January 1998 to October 2005 were retrospectively analyzed.
RESULT:
Sixty-two patients with rhinogenous ophthalmocele disease, 18 frontal-ethmoid sinus cystic, 12 nasosinusitis, 6 fungal frontal sinusitis, 10 maxillary sinus carcinoma, 4 olfactory nerve tumour, 6 traumatic carotid cavernous fistula, 6 ethmoidal sinus osteoma. The rhinogenous ophthalmocele caused by frontal-ethmoid sinus cystic and nasosinusitis and ethmoidal sinus osteoma were cured. The maxillary sinus carcinomas were followed up for 5 years, 2 examples are alive, 2 examples are lost. The olfactory nerve tumours were death in 2 years after operation. The 2 traumatic carotid cavernous fistula were death, 4 were cured.
CONCLUSION
The disease with rhinogenous ophthalmocele was easily misdiagnosed for the low incidence of the disease. According to eyes reasons of ophthalmocele, choose the suitable operational method, it is satisfied with the result of treatment.
Adolescent
;
Adult
;
Aged
;
Diagnostic Errors
;
Exophthalmos
;
diagnosis
;
etiology
;
Female
;
Humans
;
Male
;
Middle Aged
;
Nose Diseases
;
complications
;
diagnosis
;
Retrospective Studies
;
Treatment Outcome
;
Young Adult
9.Kimura's Disease Involving the Ipsilateral Face and Extraocular Muscles.
Sang Joon LEE ; Ju Hwan SONG ; Shin Dong KIM
Korean Journal of Ophthalmology 2009;23(3):219-223
Kimura's disease (KD) is a rare, chronic inflammatory disorder, which is characterized by tumor-like masses mainly located in the head and neck region. Extraocular muscle involvement in KD is uncommon. We report a case of KD that involved both the extraocular muscles and buccal area. A 13-year-old male presented to our clinic with a two-year history of exophthalmos of the left eye and facial swelling. Facial CT and MRI showed a 1.5 x 1.5 cm2 soft tissue mass located at the left masticator and buccal area, exophthalmos of the left eye, and diffuse thickening of the left extraocular muscles. We performed a lateral rectus muscle incisional biopsy of the left eye. Oral methylprednisolone therapy was initiated and tapered following the incisional biopsy.
Administration, Oral
;
Adolescent
;
Angiolymphoid Hyperplasia with Eosinophilia/complications/*diagnosis/drug therapy/surgery
;
Cheek/*pathology
;
Edema/etiology
;
Exophthalmos/etiology
;
Face
;
Glucocorticoids/administration & dosage
;
Humans
;
Magnetic Resonance Imaging
;
Male
;
Methylprednisolone/administration & dosage
;
Oculomotor Muscles/*pathology/surgery
;
Postoperative Care
;
Treatment Outcome
10.A Case of Complete Ophthalmoplegia in Herpes Zoster Ophthalmicus.
Hyun Min SHIN ; Helen LEW ; Young Su YUN
Korean Journal of Ophthalmology 2005;19(4):302-304
PURPOSE: To report a case with complete ophthalmoplegia after herpes zoster ophthalmicus. METHODS: A 70-year-old male patient visited a clinic because of vesicular eruptions over the left side of his face with severe pain. Drooping and severe swelling of the left eyelid were present, along with keratitis and uveitis. While the lid swelling and uveitis were improving, external ophthalmoplegia and exophthalmos were discovered. Intramuscular injections of dexamethasone 5 mg were given for 10 days, followed by oral administration of prednisolone at a dosage of 15 mg for two weeks and 10 mg for two weeks. RESULTS: The patient was fully recovered from the complete ophthalmoplegia and exophthalmos six months after the onset of the cutaneous lesion. CONCLUSIONS: Complete ophthalmoplegia is a rare ophthalmic complication of herpes zoster infection. Therefore, an evaluation of extraocular muscle and lid function should be performed during the examination of herpes zoster patients in order to screen for ophthalmoplegia.
Severity of Illness Index
;
Prednisolone/therapeutic use
;
Ophthalmoplegia/drug therapy/*etiology
;
Male
;
Humans
;
Herpes Zoster Ophthalmicus/*complications/drug therapy
;
Glucocorticoids/therapeutic use
;
Follow-Up Studies
;
Exophthalmos/drug therapy/etiology
;
Aged