17 research outputs found

    Comparing the effect of unfractionated heparin and low molecular weight heparin in preventing of deep vein thrombosis prophylaxis after craniotomy in patients with brain tumor

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    کرانیوتومی با توجه به مستعد کردن بیماران به بی حرکتی، پس از عمل عاملی خطرساز برای ایجاد ترومبوز وریدی محسوب می شود. هدف از مطالعه حاضر مقایسه اثر دو روش درمان رایج برای پیشگیری از ترومبوز وریدی شامل هپارین معمولی ((unfractionated و هپارین با وزن مولکولی کم (کلگزان) در پیشگیری از این عارضه است. روش بررسی: در این کارآزمایی بالینی تصادفی و دوسوکور که از سال 1387 تا 1389 در اصفهان انجام شد، تعداد 154 بیمار که به علت تومور مغزی مورد عمل جراحی کرانیوتومی قرار گرفته در دو گروه تقسیم و مورد مطالعه قرار گرفتند. در گروه اول از 48 ساعت بعد از عمل کلگزان به میزان mg/d 40 به صورت زیرجلدی تجویز شد. بیماران در گروه دوم از 48 ساعت بعد از عمل، هپارین unfractionated به میزان IU/12h 5000 به صورت زیرجلدی دریافت کردند و نتایج در نرم افزار با کمک آزمون های T-test و Chi-Square مورد تجزیه و تحلیل قرار گرفتند. یافته ها:در این مطالعه تفاوت آماری معنی داری از نظر سن، جنس و بیماری های زمینه ای بین دو گروه مشاهده نشد (05/0P>). طی مطالعه 14 مورد (2/18) ترومبوز وریدهای عمقی تحت بالینی در گروه هپارین و 3 مورد (9/3) در گروه کلگزان مشاهده شد (011/0=P). هیچکدام از بیماران در پیگیری پس از کرانیوتومی دچار خونریزی داخل مغزی نشدند. نتیجه گیری: نتایج مطالعه حاضر نشان می دهد که کلگزان نسبت به هپارین unfractionated در پیشگیری از ترومبوز ورید عمقی پس از کرانیوتومی در بیماران مبتلا به تومور مغزی مؤثرتر و ایمن تر است

    Randomized study comparing the efficacy of a self-retaining bicanaliculus intubation stent with Crawford intubation in patients with canalicular obstruction

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    Syed Ziaeddin Tabatabaie, Mohammad Taher Rajabi, Mohammad Bagher Rajabi, Bahram EshraghiEye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, IranBackground: The purpose of this study was to compare the efficacy of self-retaining stent (SRS) bicanalicular intubation with bicanalicular silicone (Crawford) intubation in patients with canalicular and punctal obstruction.Methods: In this prospective, randomized clinical trial, 38 patients with canalicular or punctal obstruction (25 partial, 13 complete) and epiphora were randomized into two groups. Twenty-one patients (14 with partial and seven with complete obstruction) underwent SRS intubation and 17 patients underwent bicanalicular silicon intubation in a randomized fashion.Results: After a mean follow-up of 6 months following tube removal, 16 (76%, 12 partial, four complete) of the 21 eyes in the SRS intubation group and 13 (76%, 10 partial, three complete) in the bicanalicular silicon intubation group had a successful outcome and remained symptom-free. For partial obstructions, the success rate was 85% and 90% for the SRS and bicanalicular silicon intubation groups, respectively. The corresponding values for complete obstruction were 63% and 50% for the SRS and bicanalicular silicon intubation groups, respectively.Conclusion: SRS could effectively substitute for a more extensive procedure such as bicanalicular silicon intubation in patients with canalicular obstruction, particularly those with partial obstruction. The newly developed SRS intubation procedure has the advantages of simple, easy implementation and extubation, low cost, and a lower rate of trauma when compared with bicanalicular silicon intubation.Keywords: self-retaining bicanalicular intubation, Crawford intubation, canalicular obstructio

    Donkey Bite Leading to a Catastrophic Outcome: Bilateral Visual Loss

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    In this report we present a case of severe facial injury due to a donkey bite. Immediate repair with surgical flaps was performed. No significant complication was observed at the time of surgery or during follow up and the result was acceptable. Animal bites are relatively frequent and most often are done by dogs. Besides dogs, other animals such as cats, horses and donkeys may be responsible for this type of injuries. Although donkey bites to the facial area are very rare, they can cause severe and life-threatening injuries. Early management of facial injuries caused by animal bites is acceptable nowadays and guarantees satisfactory outcome

    Lacrimal gland prolapse in upper blepharoplasty

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    Unusual occurrence of orbital hemangiopericytoma in the zygomatic bone of an adolescent: a case report

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    Abstract Background Hemangiopericytoma and solitary fibrous tumor are considered related variants on the same spectrum and both may essentially be the same tumor. They are infrequently encountered in the orbital region while the zygomatic bone is an extremely rare location for these neoplasms to occur. Case presentation A 14-year-old boy presented with complaint of deformity of left infraorbital area and a firm, regular mass in the region. Orbital CT scan revealed a well-defined round isodense intraosseous lesion in the lowermost portion of the lateral orbital wall (zygomatic bone), expanding the bone and protruding anteriorly and medially. MRI showed the mass to be heterogenous and strongly enhancing with contrast medium. Inferior transconjunctival orbitotomy was performed and the mass was removed. The histopathologic examination and immunohistochemistry staining results (positive for CD34, CD31 and smooth muscle actin, but negative for CD99, S100, B-cell lymphoma 2 (bcl-2) and desmin) confirmed the diagnosis of hemangiopericytoma. The postoperative course was uneventful, with no evidence of recurrence after 5 years follow up. Conclusions This case represents the second hemangiopericytoma reported in the zygomatic bone. Although extremely rare, hemangiopericytoma/solitary fibrous tumor might be considered in the differential diagnosis of intraosseous lesions of the orbital and zygomatic region

    A rare erosive orbital mass in a child: Case report of myofibroma

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    Purpose: To present the clinical, histological, and radiographic findings of a case of orbital myofibroma in an unusual location. The literature is reviewed and the clinical relevance discussed. Methods: A 5-year-old boy was examined with a 1.5-month history of progressive swelling in the left supraorbital region. Results: Examination revealed a firm, painless mass in the supralateral region of the left orbit with slight reddish discoloration of the overlying skin. Computerized tomography (CT) scan images showed a well demarcated, homogenous, solid mass with extension to the lacrimal gland region and adjacent to frontal bone erosion. The mass was surgically excised and was confirmed to be myofibroma in diagnostic histological studies. There has been no evidence of recurrence in the first year after surgery. Conclusions: Clinical appearance and imaging findings are unspecific for this tumor, and histological examination still remains the definite method of diagnosis. Therefore, it is important to be able to differentiate myofibromas from other malignant tumors with a similar presentation in pediatric patients to avoid mismanagement. Keywords: Orbital tumor, Lacrimal gland, Children, Histopatholog

    Application of ultrasound biomicro-scopy in the planning of cataract surgery in anterior megalophthalmos

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    Anterior megalophthalmos, a rare hereditary disorder, is macrocornea (horizontal corneal diameter more than 13 mm) in association with enlarged lens-iris diaphragm and ciliary ring. One of the major challenging issues in the cataract surgery of these patients is preventing intraocular lens (IOL) malposition, because of probable large capsular bag. Several approaches have been selected by previous surgeons, such as, custom-made anterior chamber IOLs. In this study, we show a normal capsular bag diameter despite ciliary ring enlargement, with application of ultrasound biomicroscopy (UMB). We suggest that in cases of anterior megalophthalmos without phacodonesis, UBM could measure the actual size of the capsular bag and obviate the need for further procedures

    Delayed retrobulbar hemorrhage after reconstruction of inferior orbital wall fracture: a case report

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    A 25-year-old man presented with enophthalmos and hypophthalmos in the left eye, underwent orbital floor reconstruction. Three days after the initial surgery, the patient’s visual acuity (VA) reduced to finger counting at 3 m, intraocular pressure increased to 32 mmHg, and relative afferent pupillary defect was detected. Further, spiral computed tomography demonstrated retrobulbar hemorrhage. After cantholysis and canthotomy, the VA was 20/200, 4 h postoperatively. Within 3 days, VA improved to 10/10. Physicians should have a heightened index of suspicion and awareness of this uncommon complication

    Horner Syndrome Following Penetrating Neck Injuries: A Case Series

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    To report three cases of Horner syndrome associated with penetrating neck injuries and the result of surgery for correcting the resulting ptosis. This is a retrospective case series study of 3 patients with Horner syndrome with past history of penetrating trauma to the neck. The patients’ history and the surgical results are presented. Muller’s muscle conjunctival resection was successfully used to treat ptosis in traumatic Horner syndrome in two cases. In the clinical setting of acute traumatic injury to the neck, careful evaluation for signs and symptoms of Horner syndrome should be performed. Horner syndrome and associated ptosis can be effectively managed using Muller’s muscle conjunctival resection.Keywords: Wounds; Penetrating; Neck; Horner Syndrome; Ptosis

    Orbicularis oculi myectomy as a treatment for blepharospasm in a case of Schwartz Jampel syndrome

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    Purpose: To describe a patient with Schwartz Jampel vel Aberfeld syndrome (SJS) who underwent orbicularis oculi myectomy as a treatment for blepharospasm. Case Report: A 4-year-old child with SJS did not respond to an injection of a single dose of botulinum toxin after one month, so orbicularis myectomy was then performed under general anesthesia. During the procedure, orbicularis vermiform movements were a useful guide for the extent of myectomy that the patient needed. He responded very well to this procedure and experienced significant relief of blepharospasm documented in follow-up visits for up to 6 months. Conclusion: Blepharospasm in patients with SJS can be treated with orbicularis oculi myectomy as a good functional method with faster and durable response in comparison to botulinum toxin injection
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