Desmoplastic Fibroma of the Mandible in a Pediatric Patient: A Case Report of Resection and Reconstruction With A Six-Year Follow-Up

2017 ◽  
Vol 75 (7) ◽  
pp. 1568.e1-1568.e10 ◽  
Author(s):  
Hernán Ramírez Skinner ◽  
Alex Vargas ◽  
Antonieta Solar ◽  
Camila Foncea ◽  
Paula Astorga
Keyword(s):  
Case Report ◽  
Pediatric Patient ◽  
Desmoplastic Fibroma

scholarly journals Desmoplastic fibroma in the proximal femur: A case report with long-term follow-up

2015 ◽  
Vol 10 (4) ◽  
pp. 2465-2467 ◽  
Author(s):  
YU-BAO GONG ◽  
LI-MEI QU ◽  
XIN QI ◽  
JIAN-GUO LIU
Keyword(s):  
Case Report ◽  
Proximal Femur ◽  
Desmoplastic Fibroma ◽  
Long Term Follow Up

scholarly journals Extended curettage and heat ablation for desmoplastic fibroma of the distal femur with a 12-year follow-up period: A case report

2014 ◽  
Vol 8 (3) ◽  
pp. 1103-1106 ◽  
Author(s):  
MASAHIRO YOKOUCHI ◽  
YOSHINORI UENO ◽  
SATOSHI NAGANO ◽  
HIROFUMI SHIMADA ◽  
SHUNSUKE NAKAMURA ◽  
...  
Keyword(s):  
Case Report ◽  
Distal Femur ◽  
Desmoplastic Fibroma ◽  
Extended Curettage

scholarly journals Case Report: Rosai-Dorfman Disease Involving Sellar Region in a Pediatric Patient: A Case Report and Systematic Review of Literature

2020 ◽  
Vol 7 ◽  
Author(s):  
Yi Zhang ◽  
Jie Liu ◽  
Jianyu Zhu ◽  
Xiang Zhou ◽  
Kun Zhang ◽  
...  
Keyword(s):  
Systematic Review ◽  
Case Report ◽  
Pediatric Patient ◽  
Cervical Lymphadenopathy ◽  
Sellar Region ◽  
Rosai Dorfman Disease ◽  
The Individual ◽  
Mass Lesions ◽  
Endocrine Abnormality

Rosai-Dorfman disease (RDD) is an extremely rare histiocytic disorder characterized by cervical lymphadenopathy, while the involvement of sellar region is less observed. Here we report a pediatric patient who was initially suspected as sellar germinoma but later identified as RDD. We also conducted a systematic review about RDD involving sellar region. A total of only 14 cases were included and analyzed in our study in terms of clinical presentation, endocrine abnormality, radiological features, pathology, treatment, and follow up. The most common neurological manifestations of sellar RDD is diabetes insipidus and visual changes. Two typical kinds of MRI manifestations were presented in sellar RDD; one is like meningioma-like mass lesions, another showing infiltrative pattern that demonstrates hyperintense areas on T2WI. Currently, the treatment of RDD is tailored to the individual clinical circumstances. For sellar RDD, surgical treatment can be considered to completely remove or debulk the tumor.

Inverted ILM Flap Technique in a Pediatric Traumatic Macular Hole—A Case Report

2017 ◽  
Vol 1 (5) ◽  
pp. 338-340 ◽  
Author(s):  
Tommaso Nuzzo ◽  
Fabio Patelli ◽  
Giovanni Esposito ◽  
Leonardo Colombo ◽  
Luca Rossetti
Keyword(s):  
Visual Acuity ◽  
Case Report ◽  
Macular Hole ◽  
Pediatric Patient ◽  
Pars Plana Vitrectomy ◽  
Flap Technique ◽  
Initial Visual Acuity ◽  
Counting Finger ◽  
Pars Plana

Purpose: To report and describe the clinical course of a pediatric traumatic macular hole (TMH) case and its management. Case Report: A pediatric patient presented a macular hole following blunt ocular trauma. The patient was followed every 2 weeks for 4 months. After the worsening of the macular hole reported by optical coherence tomography (OCT), pars plana vitrectomy with inverted flap technique plus SF6 gas tamponade was performed. Traumatic macular hole appeared closed at the OCT during follow-up. Initial visual acuity was counting finger at 30 cm. After surgery, the patient achieved a visual acuity of 20/100 at 3-month follow-up. Conclusion: This case shows a good anatomic and functional success performing a pars plana vitrectomy with inverted flap technique in a large TMH in a pediatric patient. We underline the importance of the surgical timing in the management of similar cases.

scholarly journals Pediatric bladder neuroblastoma: Case report and literature review

2013 ◽  
Vol 7 (9-10) ◽  
pp. 609 ◽  
Author(s):  
Justin Zhu ◽  
Nathan Hoag ◽  
Paul Gustafson ◽  
Kourosh Afshar ◽  
Andrew MacNeily
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Literature Review ◽  
Pediatric Patient ◽  
Partial Cystectomy ◽  
Gross Hematuria ◽  
Rare Neoplasm ◽  
Rare Diagnosis

Neuroblastoma (NBL) of the urinary bladder is an extremely rare diagnosis, with only 6 cases reported in the literature to date. We report the case of a 3-year-old boy who presented with gross hematuria, and was diagnosed with bladder NBL after partial cystectomy. Two-year follow-up has been unremarkable. This case highlights a rare neoplasm of the urinary bladder in a pediatric patient.

scholarly journals Radiotherapy for Desmoplastic Fibroma of Bone: A Case Report

2003 ◽  
Vol 11 (1) ◽  
pp. 90-93 ◽  
Author(s):  
HL Nag ◽  
R Kumar ◽  
S Bhan ◽  
BS Awasthy ◽  
PK Julka ◽  
...  
Keyword(s):  
Case Report ◽  
Relevant Literature ◽  
Benign Tumour ◽  
Treatment Modalities ◽  
Histopathological Diagnosis ◽  
Desmoplastic Fibroma ◽  
Surgical Options ◽  
Rare Benign Tumour

Desmoplastic fibroma is a rare benign tumour of bone. Diagnosis is not easy and is often made by excluding other tumours. Histopathological diagnosis of this tumour is also sometimes not easy. The treatment modalities for this tumour are non-uniform and often controversial. In the present case surgical options were left aside because the patient did not consent to surgery, so radiotherapy was used, with success at 3-year follow-up. This case is presented here along with a review of relevant literature.

scholarly journals Low-Energy Multilevel Vertebral Fracture in a Pediatric Patient during Follow-up for Idiopathic Hypercalciuria: A Case Report

2015 ◽  
Vol 21 (3) ◽  
pp. 137-140
Author(s):  
Emine Eda Kurt ◽  
Zeliha Güzelküçük ◽  
Fatmanur Aybala Koçak ◽  
Hatice Rana Erdem ◽  
Figen Tuncay
Keyword(s):  
Case Report ◽  
Vertebral Fracture ◽  
Pediatric Patient ◽  
Low Energy ◽  
Idiopathic Hypercalciuria

Intensive Stuttering Therapy With Telepractice Follow-up: A Case Study

2011 ◽  
Vol 21 (1) ◽  
pp. 11-21 ◽  
Author(s):  
Farzan Irani ◽  
Rodney Gabel
Keyword(s):  
Case Report ◽  
Therapeutic Intervention ◽  
Intensive Therapy ◽  
Positive Outcome ◽  
Eclectic Approach

This case report describes the positive outcome of a therapeutic intervention that integrated an intensive, residential component with follow-up telepractice for a 21 year old male who stutters. This therapy utilized an eclectic approach to intensive therapy in conjunction with a 12-month follow-up via video telepractice. The results indicated that the client benefited from the program as demonstrated by a reduction in percent stuttered syllables, a reduction in stuttering severity, and a change in attitudes and feelings related to stuttering and speaking.

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