scholarly journals Perawatan Ameloblastoma Rekuren dengan Metode Dredging

2016 ◽  
Vol 19 (1) ◽  
pp. 160
Author(s):  
R. Rahardjo

Latar belakang. Ameloblastoma dapat menyebabkan kerusakan pada tulang wajah baik pada maksila maupun mandibula. Tumor ini dapat mengalami rekurensi apabila perawatan tidak sempurna. Reseksi pada tulang yang terkena adalah tindakan yang biasa dilakukan untuk perawatan tumor ini. Tindakan ini dapat menyebabkan gangguan maloklusi, gangguan pertumbuhan dan perkembangan gigi dan tulang rahang bila dilakukan pada anak-anak dan remaja, gangguan estetika, dan berdampak psikologis. Oleh karena itu tindakan alternatif dalam perawatan ameloblastoma adalah dengan metode dredging. Tujuan laporan kasus ini menjelaskan perawatan metode dredging pada rekuren ameloblastoma pada penderita laki-laki usia dua puluh tujuh tahun sehingga dapat menghilangkan dampak psikologis dari penderita. Kasus. Penderita laki-laki usia dua puluh tujuah tahun dengan keluhan benjolan dalam mulut, tidak terasa sakit, dan merasa bertambah besar. Terdapat asimetri wajah di sebelah kanan, tidak ada perubahan warna kulit. Penderita mengaku pernah dioperasi tujuh tahun yang lalu. Pada pemeriksaan intra oral didapatkan benjolan pada mandibula di daerah bukal dari daerah gigi 42 sampai 46. Pada palpasi terasa ada fluktuasi, rasa sakit ringan dan warna mukosa normal. Pada gambaran foto panoramic terlihat area radiolusen dengan batas jelas dari daerah 42 sampai 46 dengan melibatkan aspek dari gigi 42 dan 43. Dari hasil biopsi dan pemeriksaan patologi anatomi dinyatakan sebagai ameloblastoma unikistik tipe folikuler. Penatalaksanaan. Dredging dikerjakan dengan melakukan defleksi pada lesi enukleasi dan kuretase. Pada bulan kedua perawatan tindakan tersebut diulangi dan dilakukan pemeriksaan histopatologis. Tindakan tersebut diulang pada bulan kelima dan diulang kembali setiap tiga bulan sampai dinyatakan terbebas dari sel tumor. Kesimpulan. Telah dilakukan dredging pada penderita rekuren ameloblastoma dengan hasil cukup memuaskan dan dilakukan pengamatan yang berlanjut. Background. Ameloblastoma can destruct the facial bones both the maxilla and mandible. The appearance of recurrent tumor is occured if the tumor is not totally removed. The resection of the affected bone is the common treatment of the tumor. These treatment lead complications such as malocclusion, abnormaldental and jaws development especially in children and adolescents, aesthetic problems, and psychological depressions. Therefore, the alternative treatment of it tumor is dredging method. Objection. This case report describe that dredging method treatment on recurrent ameloblastoma on male patient aged twenty seven years old, can eliminate patients’s psychological depressions. Case. Male patient aged twenty seven years old has a lump problem in mouth, painless, and has progressive enlargement, asymmetry on the right face, no change in skin color. Patients admitted to surgery seven years ago. On intra oral examination found a lump in the mandible in buccal area of the tooth 42 to 46. On palpation examination, there were fluctuations, mild pain and normal color mucosa. The panoramic photograph was found radiolucent area with clear boundaries of the region 42 to 46 by engaging aspect of teeth 42 and 43. The results of hispathology examination assessed a unicystic amelobastoma follicular type. Treatment. Dredging method was done by performing enucleation and consecutive curettage. Second month after the first treatment, the enucleation and the curettage was repeated then need histopathological examination. The treatment was repeated again in fifth month after the first treatment repeated every three months until histopathological examination declared free of tumor cells. Conclusion. Dredging has been performed on two patients with ameloblastoma with satisfactory results and continued observation.

2015 ◽  
Vol 2015 ◽  
pp. 1-4 ◽  
Author(s):  
Zerrin Unal Erzurumlu ◽  
Peruze Celenk ◽  
Emel Bulut ◽  
Yakup Sancar Barıs

Fibrous dysplasia is a benign fibroosseous bone dysplasia that can involve single (monostotic) or multiple (polyostotic) bones. Monostotic form is more frequent in the jaws. It is termed as craniofacial fibrous dysplasia, when it involves, though rarely, adjacent craniofacial bones. A 16-year-old girl consulted for a painless swelling in the right posterior mandible for two years. Panoramic radiography revealed ground-glass ill-defined lesions in the three different regions of the maxilla and mandible. Axial CT scan (bone window) showed multiple lesions involving skull base and facial bones. Despite lesions in the skull base, the patient had no abnormal neurological findings. The lesion was diagnosed as fibrous dysplasia based on radiological and histopathological examination. In this paper, CT findings and differential diagnosis of CFD are discussed. CT is a useful imaging technique for CFD cases.


VASA ◽  
2011 ◽  
Vol 40 (3) ◽  
pp. 251-255 ◽  
Author(s):  
Gruber-Szydlo ◽  
Poreba ◽  
Belowska-Bien ◽  
Derkacz ◽  
Badowski ◽  
...  

Popliteal artery thrombosis may present as a complication of an osteochondroma located in the vicinity of the knee joint. This is a case report of a 26-year-old man with symptoms of the right lower extremity ischaemia without a previous history of vascular disease or trauma. Plain radiography, magnetic resonance angiography and Doppler ultrasonography documented the presence of an osteochondrous structure of the proximal tibial metaphysis, which displaced and compressed the popliteal artery, causing its occlusion due to intraluminal thrombosis..The patient was operated and histopathological examination confirmed the diagnosis of osteochondroma.


Author(s):  
Asma Beyki ◽  
Mahmud Zardast ◽  
Zahra Nasrollahi

Invasive aspergillosis of the paranasal sinuses is a rare and often misdiagnosed disease. This study reported a case of max- illary aspergillosis with a complete  headache and eye pain after tooth extraction with a large abscess in the relative jaw. Tenderness in the right temporal, lower jaw numbness and right eye proptosis was found. Histopathological examination was the suggestion of maxillary sinusitis with a fungal ball of aspergillus.


2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Haider Alyousef ◽  
Elsawi M. Osman ◽  
Mohamed A. Gomha

Introduction. Liposarcoma is a rare pathological entity. By far it is the most common histological subtype of genitourinary sarcomas in adults. Approximately two hundred cases were reported in the literature. We are hereby presenting a case with a typical clinical scenario of paratesticular liposarcoma.Case report. A 75-year-old gentleman presented with a painless right hemiscrotal swelling that was progressively increasing in size over the last 6 years. Testicular tumour markers were negative. Imaging showed a heterogenous mass with fat component. Subsequently he underwent wide local excision that included the paratesticular mass along with the right testicle and all right inguinal canal contents up to the deep inguinal ring with the sparing of right illioinguinal nerve. Histopathological examination showed a well differentiated liposarcoma of the spermatic cord. He remained recurrence-free so far after 18 months of followup.Conclusion. Radical orchidectomy with wide local excision comprises the cornerstone of treatment of paratesticular liposarcoma. Due to the rarity of the disease there is no definite universal consensus of opinion as regards the role of radiotherapy and chemotherapy.


BMC Surgery ◽  
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Wen Ai ◽  
Zhihua Liang ◽  
Feng Li ◽  
Haihua Yu

Abstract Background The common complications of radical hysterectomy and pelvic lymphadenectomy usually include wound infection, hemorrhage or hematomas, lymphocele, uretheral injury, ileus and incisional hernias. However, internal hernia secondary to the orifice associated with the uncovered vessels after pelvic lymphadenectomy is very rare. Case presentation We report a case of internal hernia with intestinal perforation beneath the superior vesical artery that occurred one month after laparoscopic pelvic lymphadenectomy for cervical cancer. A partial ileum resection was performed and the right superior vesical artery was transected to prevent recurrence of the internal hernia. Conclusions Retroperitonealization after the pelvic lymphadenectomy should be considered in patients with tortuous, elongated arteries which could be causal lesions of an internal hernia.


2002 ◽  
Vol 120 (5) ◽  
pp. 154-157 ◽  
Author(s):  
Eduardo Toledo de Aguiar ◽  
Alex Lederman ◽  
Patrícia Matsunaga

CONTEXT: Total occlusion of the common carotid is rare and the indications and techniques for surgical treatment are still a matter of controversy. OBJECTIVE: To demonstrate the feasibility of retrograde common carotid endarterectomy. DESIGN: Retrospective case report study. SETTING: Tertiary care private hospital. PARTICIPANTS: Three patients underwent ring-stripping retrograde common carotid endarterectomy. Their ages were 81, 68 and 65 years. All were hypertensive with generalized atherosclerosis, two had diabetes mellitus, and one had undergone coronary artery bypass some years earlier and had non-dialytic chronic renal insufficiency. Symptoms of brain ischemia were present in two patients. All patients had total occlusion of the common carotid, extending from the origin to the bifurcation and localized in the right common carotid in two cases. In two cases the internal carotid artery was also occluded. MAIN MEASUREMENTS: Postoperative early mortality and stroke rate, and the medium and long-term endarterectomy patency. RESULTS: There were no deaths. One patient had a transient ischemic attack. All endarterectomies were patent after eight months, four years and seven years of follow-up. CONCLUSION: There is low mortality, and the procedure can be done through only one cervical incision. Tandem lesions of the carotid arteries can be treated together. It is suitable for long total occlusions of the common carotid, and long-term patency.


2013 ◽  
Vol 39 (5) ◽  
pp. 609-614
Author(s):  
Sema Murat ◽  
Ayhan Gurbuz ◽  
Kivanc Kamburoglu

This case report details a 65-year-old male patient who underwent mandibular resection and radiotherapy as treatment for squamous cell carcinoma of the right mandible. The patient was rehabilitated with an implant-supported fixed partial denture and a maxillary occlusal ramp. The patient has been wearing his prosthesis for 2 years with no complaints.


2010 ◽  
Vol 46 (2) ◽  
pp. 138-142 ◽  
Author(s):  
Marjorie E. Milne ◽  
Christina McCowan ◽  
Ben P. Landon

Spontaneous pneumothorax is rarely reported in the cat. This case report describes the use of computed tomography (CT) to diagnose pulmonary bullae in an adult cat with recurrent spontaneous pneumothorax. A large bulla in the right middle lung lobe and several blebs in other lobes were identified by CT. Partial lobectomy of the right middle and right and left cranial lung lobes was successfully performed to remove the affected portions of lung. Histopathological examination suggested bronchopulmonary dysplasia (BPD) as the underlying cause for development of the pulmonary bulla. This is the first case report in the veterinary literature describing the use of CT to identify pulmonary bullae in the cat with BPD as a possible underlying cause.


2008 ◽  
Vol 12 (4) ◽  
pp. 180-183 ◽  
Author(s):  
Mike S. Kalisiak ◽  
Richard M. Haber

Background: Angioma serpiginosum is a vascular anomaly that classically presents in childhood and predominantly affects females. Objective: To present a case of a young woman with linear distribution of angioma serpiginosum and review the common clinical characteristics and presentation of this condition. Methods: Case report with skin biopsies and dermoscopic findings. Results: A clinical examination revealed numerous irregular punctate red macules in a linear distribution over the right arm. On dermoscopy, the lesions appeared as multiple sharply demarcated red lagoons. The histopathologic findings of dilated blood vessels in the papillary dermis with absence of other changes confirmed the diagnosis of angioma serpiginosum. Conclusion: Angioma serpiginosum is a rare entity that can be distinguished by clinical and histopathologic examinations. Lack of recognition of this condition may lead to unnecessary investigations and delayed treatment.


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