scholarly journals A sacrococcygeal teratoma-a rare entity among adult males: a case report and review of literature

2021 ◽  
Vol 8 (5) ◽  
pp. 1646
Author(s):  
Suhail M. Khan ◽  
Azhar A. Khan ◽  
Anzeen N. Kanth ◽  
Aymen M. Khan ◽  
Irfita N. Kanth
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Germ Cell ◽  
Sacrococcygeal Teratoma ◽  
Rare Entity ◽  
Adult Males ◽  
Review Of Literature ◽  
Old Adult ◽  
Cell Layers ◽  
Congenital Tumours

Sacrococcygeal teratoma (SCT) is derived from embryonic germ cell layers and is one of the commonest tumours in infants. It is the most commonly occurring solid congenital tumours in the foetus and the new born. It is very rare in adults with less than a hundred cases documented in literature, with even rarer cases of male presentation. We report a case of a 26-year-old adult male presenting with a sacrococcygeal teratoma who was treated in our hospital along with its literature review.

Vaginal Leiomyoma: Case Report and Literature Review

2017 ◽  
Vol 5 (1) ◽  
pp. 62-65
Author(s):  
Mamta Gupta ◽  
Rita Jindal ◽  
Supriya Kumari ◽  
Namrata Nargotra
Keyword(s):  
Case Report ◽  
Literature Review ◽  
South Asian ◽  
Coming Out ◽  
Rare Entity ◽  
Review Of Literature ◽  
Vaginal Route ◽  
The Right ◽  
Vaginal Leiomyoma

ABSTRACT Introduction Leiomyoma arising from the vagina is a rare entity with varied presentations. Case Report A woman 44 years of age presented with complaints of something coming out vaginally, polymenorrhea, and pain in abdomen. A mass arising from the right posterolateral wall of vagina was seen. Ultrasound reported it to be cervical fibroid. The mass was enucleated through vaginal route. Histopathology confirmed it to be a leiomyoma. Review of literature revealed that it has a varied presentation. Diagnosis is often missed. Conclusion The condition should always be kept in mind whenever coming across any mass in vagina. How to cite this article Gupta M, Saini V, Jindal R, Kumari S, Nargotra N. Vaginal Leiomyoma: Case Report and Literature Review. J South Asian Feder Menopause Soc 2017;5(1):62-65.

scholarly journals Sacrococcygeal Teratoma in a Teen - A Case Report

1970 ◽  
Vol 16 (2) ◽  
pp. 76-78 ◽  
Author(s):  
Md K Rahman ◽  
SMM Haq ◽  
AK Sarker ◽  
SMA Shahid ◽  
MB Islam
Keyword(s):  
Case Report ◽  
Germ Cell ◽  
Sacrococcygeal Teratoma ◽  
Sacrococcygeal Region ◽  
Cell Layers ◽  
Congenital Neoplasm

Sacrococcygeal teratoma is a common congenital neoplasm. This tumor contains derivatives ofmore than one of the three embryonic germ cell layers e.g. ectoderm, mesoderm & endodermand usually arises as a mass in the sacrococcygeal region. Here we are reporting a case of hugesacrococcygeal teratoma presenting as a lower abdominal and perineal mass in a thirteen-yearoldschoolgirl, which is very rare.doi: 10.3329/taj.v16i2.3888TAJ December 2003; Vol.16(2): 76-78

scholarly journals Lipoma of the Larynx: Our Experience

2016 ◽  
Vol 6 (2) ◽  
pp. 89-92
Author(s):  
Nupur Kapoor Nerurkar ◽  
Ankit A Jain ◽  
Binhi H Desai
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Surgical Excision ◽  
Accurate Diagnosis ◽  
Differential Diagnoses ◽  
Rare Entity ◽  
Review Of Literature ◽  
Management Protocol ◽  
Custom Made ◽  
Slow Growing

ABSTRACT Objective Four cases of laryngeal lipoma are presented with a discussion of their differential diagnoses and management. Materials and methods Case report and literature review. Results Laryngeal lipomas, though a fairly rare entity, are occasionally the cause of persistent hoarseness of voice. An accurate diagnosis is important and the management may vary from surgical excision to only wait and watch policy, as these tumors are usually slow growing. A discussion of the presentation and management of four cases of laryngeal lipoma managed by us is documented with a review of literature. Conclusion Laryngeal lipomas have no set management protocol. A custom-made plan for each patient should be charted out depending on the symptoms of the patient and extent of the lipoma. How to cite this article Nerurkar NK, Jain AA, Desai BH. Lipoma of the Larynx: Our Experience. Int J Phonosurg Laryngol 2016;6(2):89-92.

Large Adult Sacrococcygeal Teratoma: A Case Report And Review Of Literature

2011 ◽  
Vol 1 (5) ◽  
pp. 164-165
Author(s):  
Dr. Yavalkar PA Dr. Yavalkar PA ◽  
◽  
Dr. Naik AM Dr. Naik AM
Keyword(s):  
Case Report ◽  
Sacrococcygeal Teratoma ◽  
Review Of Literature ◽  
Large Adult

scholarly journals Idiopathic ovarian vein thrombosis causing pulmonary embolism: case report and literature review

2021 ◽  
Vol 49 (6) ◽  
pp. 030006052110106
Author(s):  
Wenrui Li ◽  
Saisai Cao ◽  
Renming Zhu ◽  
Xueming Chen
Keyword(s):  
Computed Tomography ◽  
Pulmonary Embolism ◽  
Abdominal Pain ◽  
Case Report ◽  
Literature Review ◽  
Ovarian Vein ◽  
Review Of Literature ◽  
Vein Thrombosis ◽  
Medical Disorder ◽  
Ovarian Vein Thrombosis

Ovarian vein thrombosis (OVT) is a rare medical disorder, which is most often found in the immediate postpartum period. OVT is rarely considered idiopathic. We report a case of idiopathic OVT with pulmonary embolism in a 33-year-old woman who presented with abdominal pain. Computed tomography and postoperative pathology confirmed the diagnosis of idiopathic OVT. To date, only 12 cases of idiopathic OVT have been reported. In this case report, we present a summary of these cases and a review of literature regarding management of idiopathic OVT.

Bullosis Diabeticorum in a Young Child: Case Report of a Very Rare Entity and a Literature Review

2017 ◽  
Vol 41 (2) ◽  
pp. 129-131 ◽  
Author(s):  
Anca Chiriac ◽  
Irina Costache ◽  
Cristian Podoleanu ◽  
Adrian Naznean ◽  
Simona Stolnicu
Keyword(s):  
Case Report ◽  
Young Child ◽  
Literature Review ◽  
Rare Entity ◽  
Bullosis Diabeticorum

scholarly journals Renal papillary hypertrophy, a rare cause of recurrent gross hematuria; Case report and review of literature

2020 ◽  
Vol 92 (4) ◽  
Author(s):  
Ahmad Beltagy ◽  
Mohamed Elsaqa ◽  
Islam Koraiem ◽  
Ahmed Abulfotooh Eid
Keyword(s):  
Case Report ◽  
Laser Ablation ◽  
Literature Review ◽  
Minimally Invasive ◽  
Active Bleeding ◽  
Review Of Literature ◽  
Gross Hematuria ◽  
Holmium:Yag Laser ◽  
Invasive Management

Hematuria is a critical symptom that should properly be investigated. One of the rare causes is renal papillary hypertrophy. Literature review revealed only few reported cases. Biopsy in reported cases has shown hyperplasia of renal papillae with normal histology. We report a case of bilateral renal papillary hypertrophy in a 32 years old female presented with intermittent gross hematuria. Computed tomgraphy urography, cystoscopy and selective cytology did not show any positive findings. Retrograde flexible uretero-renoscopy showed enlarged renal papillae protruding into upper and middle calyces of both kidneys with clots and active bleeding in some. Holmium:YAG Laser ablation of hypertrophic papillae showed an effective minimally invasive management of the condition.

scholarly journals Lateral Swivel Dislocation of the Hindfoot : A Case Report and Literature Review

2015 ◽  
Vol 2 (1) ◽  
pp. 41-43
Author(s):  
Rajesh Kapila ◽  
Partap singh Verka ◽  
Radhe sham Garg ◽  
Mannan Ahmed
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Subtalar Joint ◽  
Asia Pacific ◽  
Talonavicular Joint ◽  
Review Of Literature ◽  
Rare Type ◽  
Present Case Report ◽  
Comprehensive Review ◽  
Type Of Injury

ABSTRACT Lateral swivel dislocation, a subtype pattern of dislocations occurring at mid tarsal joint is a rare type of injury. A medially or laterally directed force applied to the forefoot causes dislocation of the talonavicular joint but not subtalar joint. The calcaneum alongwith the remaining foot swivels on the intact interosseous talocalcaneal ligament. The present case report is a more rare lateral swivel type of dislocation of talonavicular joint in a 25-year-old male. The article also presents a comprehensive review of literature and management of such type of injuries of the hindfoot . How to cite this article Kapila R, Verka Ps, Garg Rs, Ahmed M. Lateral Swivel Dislocation of the Hindfoot: A Case Report and Literature Review. J Foot Ankle Surg (Asia-Pacific) 2015;2(1): 41-43.

scholarly journals Post Traumatic Biparietal Mirror Extradural Haematoma – A Case Report and Review of Literature

2018 ◽  
Vol 32 (3) ◽  
pp. 458-461
Author(s):  
G. Venkateswara Prasanna ◽  
Sathish Kumar Vandanapu ◽  
Hima Bindu
Keyword(s):  
Case Report ◽  
Postoperative Period ◽  
Emergency Evacuation ◽  
Extradural Haematoma ◽  
Rare Entity ◽  
Review Of Literature ◽  
Careful Planning ◽  
Cerebral Trauma ◽  
Post Traumatic ◽  
Extradural Haematomas

Abstract Bilateral extradural haematomas [EDH] are rare and it is an uncommon consequense of cranio cerebral trauma. The mortality is higher than unilateral extradural haematoma and management of extradural haematomas requires careful planning, judicial surgical exposure and most important is timing of evacuation of extradural haematomas. Emergency evacuation of bilateral extradural haematomas were performed in this case with uneventful postoperative period. The pathophysiology and surgical nuances of this rare entity been discussed.

scholarly journals Mature sacrococcygeal teratoma: A case report and literature review

2004 ◽  
Vol 23 (2) ◽  
Author(s):  
AMO Shonubi ◽  
AA Musa ◽  
O Akiode ◽  
BA Salami ◽  
HJC Kingu ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Sacrococcygeal Teratoma
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