Academic literature on the topic 'In-toto surgery'

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Journal articles on the topic "In-toto surgery"

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Poulsen, Christine Borup, Jon Kaspersen, Carsten Reidies Bjarkam, and Søren Peter Eiskjær. "Case Report of a Hemangioblastoma Originating from the T1 Spinal Nerve Treated with in Toto Resection, Hemicorporectomy and Pedicle Screw Stabilization." Journal of Orthopaedic Case Reports 14, no. 5 (2024): 115–20. http://dx.doi.org/10.13107/jocr.2024.v14.i05.4454.

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Introduction: Previously, only 40 cases with extradural hemangioblastoma at the spinal nerve (none at the T1 nerve root) have been described in the medical literature. In toto, resection of this hypervascular tumor is essential to avoid bleeding complications. Surgery for hemangioblastoma at the cervicothoracic junction is complex and nerve resection of the T1 results in specific neurodeficits of the hand muscles which are not well known. Case Report: A 34-year-old woman was diagnosed with a slowly growing tumor located at the left foramen T1/T2. Pressure from the tumor resulted in Horner’s syndrome and pain and paresthesia in the upper extremity. The tumor was resected in toto through a posterior midline approach and rib resection and transection of the left T1 and T2 spinal nerves. T2 hemicorporectomy and spinal stabilization were performed to gain access to and mobilize the tumor ventrally. Ptosis decreased after surgery and no neurodeficit was observed except the expected deficit (no deficit was present preoperatively) caused by the T1 resection specifically a small decrease in strength of the abductor and flexor pollicis brevis and opponens pollicis and the lateral two lumbricals. Histological examination of the tumor demonstrated a hemangioblastoma. von Hippel-Lindau disease was ruled out by genetic testing of the patient’s blood. Eight-month postoperatively, all pre-operative symptoms had decreased considerably and the radiographic examination shoved unchanged pedicle screw/rod stabilization of the cervicothoracic junction. Conclusion: Hemangioblastoma is a rare hypervascular tumor very rarely located at the spinal nerve. The tumor should be resected in toto to avoid recurrence and bleeding. In the current case, the location was at the T1 root necessitating complex surgery with laminectomies and hemicorporectomy of T2 and a posterior rib resection/thoracotomy. Spinal stabilization is mandatory. Preferably embolization should be performed preoperatively. T1 transection results in a specific neurodeficit which should be explained to the patient preoperatively. The patients should undergo genetic testing for Hippel-Lindau disease. Keywords: Hemangioblastoma, von Hippel-Lindau disease, in toto resection, hemicorporectomy, spinal nerve root T1 nerve lesion.
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Kumar, Sushil, Amit Garg, and Amit Handa. "Large Cysticercus in the Cerebellopontine Angle: Case Report." Indian Journal of Neurosurgery 07, no. 02 (2017): 147–49. http://dx.doi.org/10.1055/s-0036-1596040.

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AbstractNeurocysticercosis is an infection of the central nervous system caused by larvae of the pork tapeworm Taenia solium. We report a case of large cyst in the cerebellopontine angle that increased in size under observation and surgery revealed it to be cysticercus. It was removed in toto and patient improved on follow-up.
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Kanmani, Mani, and Chinnasamy Kasthuri. "Laparoscopic excision of accessory cavitated uterine mass and its vaginal retrieval in toto." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 10, no. 3 (2021): 1177. http://dx.doi.org/10.18203/2320-1770.ijrcog20210503.

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Accessory cavitated uterine mass (ACUM), a rare cause of dysmenorrhoea, has to be diagnosed with essential criteria and is to be treated with appropriate surgery. Hereby, presenting the surgical approach by laparoscopy and vaginal retrieval of the specimen in toto as a perfect tool. We report a rare case study of ACUM, a mullerian anomaly in a 27 years old female with severe dysmenorrhoea with secondary infertility, evaluated and diagnosed as ACUM. Preoperative diagnosis and surgical plane evaluation are made by ultrasound and magnetic resonance imaging. Hysteroscopic examination of the cavity was normal and laparoscopic excision of an ill-defined mass in the anterior and right lateral wall of 3×2 cm followed by retrieval of the specimen through a pouch of Douglas. Myometrial defect sutured. Cut section showed chocolate coloured fluid in the endometrial cavity and the same confirmed by histopathology. This is the first case report doing vaginal retrieval of ACUM in toto.
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Ilham, Pratamanugroho, and Widhiyanto Lukas. "Thoracal meningioma and neurological status recovery 6 months postoperative: A case report." World Journal of Advanced Research and Reviews 22, no. 1 (2024): 1368–70. https://doi.org/10.5281/zenodo.14222576.

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<strong>Introduction:&nbsp;</strong>Meningioma is the most common intradural tumor of the spinal cord in adults. Spinal meningioma arises from slow-growing arachnoid cap cells, which are generally located intradural extramedullary and grow laterally into the subarachnoid space to stretch the surrounding arachnoid. Local pain is usually the first major symptom. However, the majority of cases are diagnosed after the onset of neurological deficits or impaired walking. <strong>Case Presentation:&nbsp;</strong>Woman, 46 years old, with back pain radiating to both legs in the last 2 years before surgery. At 16 months before surgery, she had paralysis of both legs with bowel and bladder incontinence. Preoperative physical examination shows no muscle contraction on both lower extremities, with hypoesthesia in the Thoracal 2 dermatome. MRI examination shows intradural extramedullary mass at the level of the 2nd thoracal that compresses the entire spinal canal. Laminectomy surgery on thoracal 2 and tumor resection in toto were performed. Surgical resection showed a tumor mass of 2x1,2x1cm with a thick, spongy, brownish-yellow consistency. Histopathological examination shows psammomatous type meningioma, WHO Grade 1. The patient was discharged postoperatively with palpable muscle contractions on both legs, accompanied by no sensory abnormalities. Evaluation 1 month postoperatively, the patient was able to voluntarily move the lower extremities accompanied by the return of ability to micturate and defecate. Examination at 6 months postoperatively, the patient was able to walk without assistance and no other neurological deficit was found. <strong>Conclusion:&nbsp;</strong>Tumor resection remains as treatment of choice for spinal meningioma regardless of neurological deficit onset and histological type of tumor.
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Chen, Z. K. "An in toto DNA-database encoded “ID” system: a new concept in primary antigen recognition." Transplantation Proceedings 32, no. 7 (2000): 1865–68. http://dx.doi.org/10.1016/s0041-1345(00)01468-8.

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Vankireddi, Mahathi, Divya Bhargavi Katta, and Sowjanya Yerra. "Implantation Cyst – A Rare Occurrence after Strabismus Surgery." Delhi Journal of Ophthalmology 34, no. 1 (2024): 55–57. https://doi.org/10.4103/dljo.dljo_103_23.

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A conjunctival epithelial cyst is a rare occurrence poststrabismus surgery, with incidence ranging from 0.25% to 0.4%. This can occur when the conjunctival wound is not closed meticulously. Conjunctival epithelial cells buried beneath the conjunctival surface multiply over time creating a retention cyst. Risk factors include recessions, fornix incisions, and simple apposition of the conjunctival wound without sutures. When left untreated these cysts can enlarge and result in complications such as limitation of ocular movements, proptosis, and compression of ocular structures. This rare occurrence is underreported, and no specific management protocols have been established. Hereby, we present a case of implantation cyst developed after squint surgery. Despite meticulous surgical procedure, a retention cyst developed within 1 month of surgery. Cyst excision in toto with cauterization of the base was performed to avoid any recurrences. This case describes a rare complication of strabismus surgery and its management.
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Aydin, Yunus, Orhan Barlas, Coşkun Yolaş, et al. "Alveolar hydatid disease of the brain." Journal of Neurosurgery 65, no. 1 (1986): 115–19. http://dx.doi.org/10.3171/jns.1986.65.1.0115.

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✓ Four cases of alveolar hydatid disease of the brain encountered within 27 months in eastern Turkey are reported. All of the patients were male farmers who presented with signs of cerebral tumor. Two of the patients were shown to harbor hepatic lesions and one of them had pulmonary metastases. The cerebral lesions were removed in toto and neurological recovery was obtained in all four patients. A review of the literature revealed only five previously reported cases treated surgically. It is concluded that cerebral Echinococcus multilocularis lesions are amenable to surgery, and that their removal provides useful prolongation of life despite the presence of hepatic or pulmonary disease.
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Shah, Rishabh, Rashmi Venkatesh, Kavita Badi, and Kreena Shah. "Surgical management of intramuscular hemangioma of left masseter muscle: A case report." National Journal of Maxillofacial Surgery 15, no. 1 (2024): 160–63. http://dx.doi.org/10.4103/njms.njms_140_22.

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ABSTRACT Hemangiomas are benign soft tissue tumors which are congenital and occur due to abnormal proliferations of blood vessels. Most common location of hemangiomas is subcutaneous adipose tissue, but skeletal muscle hemangiomas are very rare which make up to 0.8% of all hemangiomas. Usually, the intramuscular lesions are common in thigh region and calf muscles and are relatively rare in the facial muscles. Long-standing lesions results in phleboliths, and this may cause some symptoms. Conventional treatment of these isolated lesions may not yield satisfactory results. Hence, surgical excision of the lesion in toto results in aesthetically pleasing results with low chances of recurrence. In this article, we report a case of a left masseter intramuscular hemangioma in 19-year-old patient which was successfully managed by complete surgical excision.
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CHACHA, B., K. SOIN, and K. C. TAN. "One Stage Reconstruction of Intercalated Defect of the Thumb Using the Osteocutaneous Radial Forearm Flap." Journal of Hand Surgery 12, no. 1 (1987): 86–92. http://dx.doi.org/10.1016/0266-7681_87_90066-0.

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A radial forearm flap including a segment of the cortex of the radius, based on the distal pedicle of the radial vessels and the cephalic vein, was used to reconstruct an intercalated defect of the thumb in two cases. In one case it was used as an ipsilateral pedicle flap while in the other case it was used as a free microvascular flap. In both cases, the skin flap as well as the segment of bone survived in toto without any evidence of creeping substitution. The functional result was good in both cases. This flap provides thin skin of good texture together with bone for a one-stage reconstruction.
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Chacha, B., K. Soin, and K. C. Tan. "One Stage Reconstruction of Intercalated Defect of the Thumb Using the Osteocutaneous Radial Forearm Flap." Journal of Hand Surgery 17, no. 6 (1992): 703. http://dx.doi.org/10.1016/0266-7681(92)90215-n.

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A radial forearm flap including a segment of the cortex of the radius, based on the distal pedicle of the radial vessels and the cephalic vein, was used to reconstruct an intercalated defect of the thumb in two cases. In one case it was used as an ipsilateral pedicle flap while in the other case it was used as a free microvascular flap. In both cases, the skin flap as well as the segment of bone survived in toto without any evidence of creeping substitution. The functional result was good in both cases. This flap provides thin skin of good texture together with bone for a one-stage reconstruction.
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Book chapters on the topic "In-toto surgery"

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Dolman, Peter J. "Surgical Exploration of the Orbit." In Surgery of the Eyelid, Lacrimal System, and Orbit. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780195340211.003.0025.

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The orbit comprises the globe and optic nerve surrounded by a complex tangle of muscles, nerves, and vessels, all cushioned in pockets of fat. While surgery in the anterior orbit is readily performed, the challenge increases significantly for deeper orbital pathology because the bony walls on four sides and the eyeball and lid structures anteriorly limit both access and visibility. The apex is a particularly difficult area because so many vital structures converge in its narrow confines. The history and physical examination help narrow the differential diagnosis so that appropriate imaging and special investigations may be arranged. The urgency of these diagnostic tests to allow appropriate medical or surgical intervention is partly determined by the speed of symptom onset and by the presence of significant pain or progressive functional impairment such as vision loss or diplopia. Computed tomography (CT) scans are usually readily available and help define the tissue characteristics and location of an orbital lesion. Reformatting allows coronal, sagittal, and 3-D views without repositioning the patient, although a true coronal CT scan may be requested if a distensible varix is suspected. Contrast CT scans may be useful for assessing the vascularity of the lesion but require an evaluation of renal function. Magnetic resonance (MR) scans may characterize certain soft tissue features better, identifying fluid levels and determining whether a lesion involves normal anatomic structures such as the optic nerve, muscle, or lacrimal gland. They are particularly useful in evaluating lesions of the optic nerve and chiasm. Ultrasounds may help to define certain superficial orbital lesions (distinguishing a lymphoma from a pleomorphic adenoma in the lacrimal gland, for example) and are very useful in assessing intraocular pathology. Positron emission tomography (PET) scans may help determine the presence of recurrent malignancy or lymphoma in a previously operated or treated site and whole body evaluation may be helpful for staging lymphomas. A trained neuroradiologist can help interpret a complex image. In general, well-circumscribed, accessible lesions are excised in toto. Poorly defined, infiltrative lesions and those causing tissue destruction (suggestive of malignancy or aggressive inflammation) usually are biopsied, either by needle or with surgery.
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Conference papers on the topic "In-toto surgery"

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Geißler, Katharina, Thomas Asendorf, Ralf Tostmann, Jan Löhler, and Orlando Guntinas-Lichius. "TOTO study: Is tonsillotomy non-inferior to tonsillectomy in children and adults with recurrent acute tonsillitis?" In 94th Annual Meeting German Society of Oto-Rhino-Laryngology, Head and Neck Surgery e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1767015.

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