An Opioid Addicted Cosmetic Patient: A Case Report and Review of the Literature for the Management of an Opioid-Dependent Cosmetic Patient

2020 ◽  
pp. 074880682093491
Author(s):  
Lara Wetton ◽  
Darryl Hodgkinson
Keyword(s):  
Chronic Pain ◽  
Case Report ◽  
Plastic Surgery ◽  
Opioid Dependence ◽  
Large Body ◽  
Evidence Based ◽  
Opioid Misuse ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Body Dysmorphia

There is a large body of literature dedicated to patient selection in plastic surgery. Much of this, however, is dedicated to the recognition of patients with body dysmorphia, those psychologically unfit for surgery, and those who have medical conditions that make the risk of complications unacceptably high. There is, however, little in the way of recognition and management of patients with chronic pain issues. With opioid misuse and dependence on the rise, the likelihood of plastic surgeons encountering patients who have obvious or occult opioid dependence issues has increased. In this case report and review of literature, we aim to present an evidence-based approach to the diagnosis and management of plastic surgery patients with a known opioid dependence.

scholarly journals Lipoma in Penis : A Rare Case Report

2013 ◽  
Vol 3 (1) ◽  
pp. 24-25
Author(s):  
T Ahmed ◽  
MA Kalam ◽  
II Mannan ◽  
MA Simi
Keyword(s):  
Case Report ◽  
Plastic Surgery ◽  
Male Patient ◽  
Rare Case ◽  
Young Male ◽  
Histopathological Analysis ◽  
Review Of The Literature ◽  
Ventral Aspect ◽  
Rare Case Report ◽  
Pedunculated Tumor

In this article we report one case of lipoma of the penis in a twenty three years old young male. This site of lipoma is rare. A case of a young male patient who consulted for removal of a penile lump is presented. The small, regular, wellcircumscribed pedunculated tumor localized on the ventral aspect of the penis was excised. The histopathological analysis showed a benign lipoma. A review of the literature showed lipoma of the penis to be very uncommon. For this reason, we were prompted to report this case.DOI: http://dx.doi.org/10.3329/bdjps.v3i1.15003 Bangladesh Journal of Plastic Surgery 2012, 3(1): 24-25

Post vasectomy chronic pain: are we under diagnosing vasitis? A case report and review of the literature

2018 ◽  
pp. 1-3 ◽  
Author(s):  
Adam Jones ◽  
Mahmood Vazirian-Zadeh ◽  
Yih Chyn Phan ◽  
Wasim Mahmalji
Keyword(s):  
Chronic Pain ◽  
Case Report ◽  
Review Of The Literature

Improving Esthetic and Functional Outcomes of Severe Habsburg Jaw Using Modified Mandibular C-Osteotomies: A Case Report and Review of Literature

FACE ◽  
2021 ◽  
pp. 273250162110482
Author(s):  
Andrew M. Henry ◽  
Jason W. Yu ◽  
Brian B. Farrell
Keyword(s):  
Case Report ◽  
Functional Outcomes ◽  
Surgical Planning ◽  
Occlusal Plane ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Clockwise Rotation ◽  
Unsatisfactory Result ◽  
Maxillary Hypoplasia ◽  
Cutting Guides

The hypoplastic mandible results in facial convergence and pseudo-prognathism. We present a patient with significant maxillary hypoplasia in both the vertical and sagittal dimensions resulting in a reverse occlusal plane. Given the significant maxillary movements required, particularly clockwise rotation, more traditional mandibular osteotomies resulted in an unsatisfactory result. A modified version to the classic “C” osteotomy with the use of surgical planning and cutting guides was performed. A review of the literature on this rarely discussed ramus osteotomy is also presented.

Development of lymphangioleiomyomatosis in a female patient with Sjö gren's disease: a review of literature and a case report

2019 ◽  
Vol 13 (2) ◽  
pp. 119-123
Author(s):  
Yu. I. Khvan ◽  
S. G. Palshina ◽  
V. I. Vasiliev
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Clinical Case ◽  
Young Female ◽  
Renal Angiomyolipoma ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
History Of ◽  
Genetically Determined ◽  
Sjögren’S Disease

Cystic and bullous lung transformation occurs in diseases of various origins: neoplastic, genetically determined, rheumatic, lymphoproliferative, and infectious diseases. The paper presents a review of the literature and a clinical case of a young female patient with a long history of Sjögren's disease. Fifteen years after the onset of the disease, the patient developed cystic and bullous lung transformation and renal angiomyolipoma, which are regarded as a manifestation of probable lymphangioleiomyomatosis.

scholarly journals Appendiceal intussusception mistaken for a polyp at colonoscopy: case report and review of literature

2010 ◽  
Vol 92 (6) ◽  
pp. e46-e48 ◽  
Author(s):  
Alireza Salehzadeh ◽  
Andrea Scala ◽  
Jay NL Simson
Keyword(s):  
Case Report ◽  
Correct Diagnosis ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Endoscopic Appearance ◽  
Appendiceal Intussusception

We report a case of appendiceal intussusception which was erroneously labelled as a 10-mm polypoid caecal lesion on colonoscopy and, therefore, followed up over an 11-year period before the correct diagnosis was made. We present the radiological and endoscopic appearance of appendiceal intussusception and a review of the literature.

Hypothenar hammer syndrome in a 22-year-old male patient: a case report and review of literature

Vascular ◽  
2011 ◽  
Vol 20 (2) ◽  
pp. 100-103 ◽  
Author(s):  
Albeir Y Mousa ◽  
Patrick A Stone ◽  
Aravinda Nanjundappa ◽  
John E Campbell ◽  
Ali F AbuRahma
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Clinical Presentation ◽  
Rare Condition ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Distal Embolization ◽  
Hypothenar Hammer Syndrome ◽  
Hand Ischemia ◽  
Complete Reversal

Hypothenar hammer syndrome is a rare condition with a peculiar presentation that aids in making a clinical diagnosis. We present a 22-year-old male patient who presented with critical hand ischemia secondary to a distal ulnar aneurysm with distal embolization. The patient was treated with an aneurysmectomy with cephalic vein interposition graft, which resulted in complete reversal of his hand ischemia. This case report outlines the clinical presentation of this rare condition, along with a recent review of the literature.

scholarly journals Granulomatous Periorificial Dermatitis in an Adult: A case report with review of literature

2020 ◽  
Vol 20 (1) ◽  
pp. 100
Author(s):  
Al-Mutasim Al-Qassabi ◽  
Khalid Al-Busaidi ◽  
Kaouthar Al Baccouche ◽  
Abla Al Ismaili
Keyword(s):  
Case Report ◽  
Rare Occurrence ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Prepubertal Children ◽  
Dermatology Clinic ◽  
Papular Eruption ◽  
Topical Metronidazole ◽  
Perioral Dermatitis ◽  
The Face

Granulomatous periorificial dermatitis (GPD) is a benign, self-limiting eruption that is considered a clinical variant of periorificial dermatitis, also known as perioral dermatitis. It presents primarily in prepubertal children as monomorphic scaly papules over perioral, paranasal and periorbital areas of the face with rare occurrence in adults. We report a 36-year-old Omani male patient who presented to the Dermatology Clinic at Bahla Polyclinic, Bahla, Oman, in 2018 with a papular eruption over his face for the previous six months. Based on clinical and histopathological findings the patient was diagnosed with GPD with sarcoid-like histology. He was treated effectively with oral doxycycline and topical metronidazole. This report provides a review of the literature on GPD and summarises all reported cases in adults to date.Keywords: Perioral Dermatitis; Dermatitis; Granulomas; Case Report; Oman.

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