enophthalmos/cefalea

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[Progressive enophthalmos in association with an orbital varix].

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BACKGROUND The orbital varix is a rare congenital disorder. Men and women are equally affected. The disease becomes usually apparent during the third decade of life. METHODS A 66-year old women presented with a history of progressive enophthalmos for the last 45 years and complained of intermittent

Bilateral enophthalmos associated with paget disease of the skull: a case report.

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OBJECTIVE To describe a case of familial Paget disease of bone associated with bilateral enophthalmos and mild exposure keratopathy. METHODS Case report and literature review. RESULTS A 71-year-old woman with familial Paget disease of bone had a long history of "receding eyes," headaches, and

Atypical Presentation of Silent Sinus Syndrome: A Case Report and Literature Review.

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Silent sinus syndrome (SSS) is a condition characterized by ophthalmologic features, such as spontaneous enophthalmos and hypoglobus with ipsilateral maxillary sinus atelectasis and an otherwise asymptomatic presentation. SSS has been documented secondary to a number of external

Silent sinus syndrome and maxillary sinus atelectasis in children.

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Silent sinus syndrome (SSS) and chronic maxillary atelectasis (CMA) are unusual conditions having subtle symptoms with a possible progressive evolution. They are particularly infrequent in the pediatric population. Our objective was to review our experience with pediatric patients having SSS or CMA,

Late sequelae after high midface trauma.

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The upper midface area comprises mainly the naso-orbito-ethmoidal (NOE) region which plays a paramount role in facial expression. Fractures of this area often result in neglected bony defects in the fragile periorbital region with major secondary impairments such as traumatic telecanthus, orbital

Silent sinus syndrome in children.

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Silent sinus syndrome (SSS) is defined as a progressive enophthalmos and hypoglobus associated with maxillary sinus atelectasis. There is extremely limited literature describing SSS in children. The goals of this study are to characterize SSS in children through an IRB approval

Not so silent sinus syndrome: A case report.

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BACKGROUND Silent sinus syndrome (SSS) is a rare disorder with protean manifestations. An absence of familiarity with ambiguous and atypical presentations may complicate diagnosis and delay management. METHODS A 28year old female patient presented with a chronic history of headache, post-nasal

[Skull base reconstruction and peroperative treatment for cranio-orbital tumors].

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OBJECTIVE To investigate the peroperative treatment of cranio-orbital tumors and the method of the reconstruction of the skull base. METHODS Between April 2008 and April 2011, 35 patients with cranio-orbital tumor were treated. There were 21 males and 14 females, aged 17-73 years (mean, 46.3 years).

Langerhans cell histiocytosis of the orbit and frontal sinus of the adult woman: A first case report in Poland.

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Langerhans cell histiocytosis (LCH) is a term describing a clonal proliferation of pathologic Langerhans cells (histiocytes), which may manifest as unisystem (unifocal or multifocal) or multisystem disease. LCH is a rare cause of the orbital tumor with the predilection to its lateral

Orbital tumors treated using transcranial approaches: surgical technique and neuroophthalmogical results in 41 patients.

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OBJECTIVE Orbital tumors can be divided schematically into primary lesions, originating from the orbit itself, and secondary lesions, extending to the orbit from neighboring structures. These tumors are variable in their biological nature and in their location. The authors evaluate 41 cases of

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