Rare case of traumatic bilateral testicular dislocation

2021 ◽  
Vol 14 (8) ◽  
pp. e244085
Author(s):  
Mude Naveen Naik ◽  
Oseen Hajilal Shaikh ◽  
Chellappa Vijayakumar ◽  
Uday Shamrao Kumbhar
Keyword(s):  
Rare Case ◽  
Inguinal Canal ◽  
Direct Impact ◽  
Associated Injuries ◽  
Imaging Studies ◽  
Motorcycle Accident ◽  
Traumatic Dislocation ◽  
Uncommon Condition ◽  
Testicular Dislocation

Bilateral traumatic testicular dislocation is an uncommon condition and usually occurs after a direct impact on the scrotum. Herein, we report this as a rare case of a 21-year-old man presenting with bilateral traumatic dislocation of testes into the inguinal canal following a motorcycle accident. Imaging studies ruled out any other associated injuries. The patient underwent bilateral orchidopexy without any further complications.

scholarly journals Bilateral Traumatic Testicular Dislocation

2018 ◽  
Vol 2018 ◽  
pp. 1-5
Author(s):  
Nubyhélia Maria Negreiro de Carvalho ◽  
Ana Clemilda Ximenes Marques ◽  
Ivon Teixeira de Souza ◽  
Vanessa Guerreiro Soares ◽  
Felipe Gomes do Nascimento ◽  
...  
Keyword(s):  
Physical Examination ◽  
Surgical Correction ◽  
Endocrine Dysfunction ◽  
Motorcycle Accident ◽  
Complete Physical Examination ◽  
Uncommon Case ◽  
Uncommon Condition ◽  
One Year ◽  
Polytrauma Patient ◽  
Testicular Dislocation

Traumatic testis dislocation is an uncommon condition and usually occurs after direct impact on the scrotum. We present an uncommon case of bilateral testicular dislocation caused by an automotive accident, which is the most frequently associated cause described in literature today. Although the fact that diagnosis can be made either by physical examination or with the use of basic exams such as Doppler ultrasound, it is not uncommon for cases to go undetected and diagnosed late. In this case, there was a late diagnosis, almost one year after the motorcycle accident. Despite this, studies describe preservation of spermatogenesis even after delayed surgical correction. The treatment can be made by manual reduction, but most of the cases need surgical correction. Therefore, it is always necessary to perform the complete physical examination of the polytrauma patient on the first medical exam, in order to avoid the risk of fertility loss, endocrine dysfunction, and future malignancy.

scholarly journals Traumatic dislocation of the testis

2019 ◽  
Vol 6 (11) ◽  
pp. 4171
Author(s):  
Bibekananda Mahapatra ◽  
Sandesh Deolekar ◽  
Pragati Singhal ◽  
Nida Khan ◽  
Manish Kumar ◽  
...  
Keyword(s):  
High Index ◽  
Testicular Function ◽  
Direct Impact ◽  
Surgical Exploration ◽  
Traumatic Dislocation ◽  
Uncommon Condition ◽  
High Index Of Suspicion

Traumatic dislocation of testis is an uncommon condition and usually occurs after direct impact on the scrotum. The diagnosis may be overlooked because of associated major injuries or due to lack of awareness of its possible occurrence. We report a case of traumatic displacement of testis in a young man presented to the emergency following polytrauma. The patient underwent a successful surgical exploration without loss of testicular function. A high index of suspicion is therefore necessary to diagnose traumatic testicular displacement.

scholarly journals Paraneoplastic polymyositis presenting as a clinically occult breast cancer

2017 ◽  
Vol 99 (2) ◽  
pp. e40-e43 ◽  
Author(s):  
N Merali ◽  
M Yousuff ◽  
V Pronisceva ◽  
A Poddar
Keyword(s):  
Paraneoplastic Syndrome ◽  
Rare Case ◽  
Primary Tumour ◽  
Imaging Studies ◽  
Occult Breast Cancer ◽  
Symptom Stability ◽  
Underlying Malignancy ◽  
Neurological Presentation ◽  
Complete History ◽  
Metaplastic Breast Carcinoma

Paraneoplastic syndrome affects less than 1% of cancer patients. Diagnosis of paraneoplastic syndrome with neurological presentation requires screening for an underlying malignancy, including a complete history, physical examination and imaging studies. Treatment often results in symptom stability, rather than improvement. Paraneoplastic polymyositis can precede or instantaneously occur at diagnosis or treatment of a primary tumour, while neurological symptoms can persist even following cancer treatment. We report a rare case of metaplastic breast carcinoma with an unusual presentation of paraneoplastic polymyositis.

scholarly journals Spinal intraosseous epidural arteriovenous fistula with perimedullary drainage obliterated with Onyx embolization: case report

2015 ◽  
Vol 23 (2) ◽  
pp. 250-253 ◽  
Author(s):  
Chang-Hsien Ou ◽  
Hao-Kuang Wang ◽  
Tzu-Hsien Yang ◽  
Cheng-Loong Liang ◽  
Ho-Fai Wong
Keyword(s):  
Case Report ◽  
Arteriovenous Fistula ◽  
Rare Case ◽  
Direct Evidence ◽  
Embolic Agent ◽  
Imaging Studies ◽  
Disease Evolution ◽  
Compressive Fracture ◽  
Rare Location ◽  
Vein Reflux

The authors report an extremely rare case of spinal intraosseous epidural arteriovenous fistula (AVF) with perimedullary vein reflux causing symptoms of myelopathy. The intraosseous fistula tracts were completely obliterated with Onyx embolic agent, resulting in a total resolution of symptoms. The unique features of this case include the rare location of the fistula in the vertebral body and the association of the fistula with a compressive fracture. Imaging studies confirmed these hemodynamic findings and provided clarity and direct evidence regarding the association of epidural AVF formation with the vertebral compressive fracture. The authors also propose a possible disease evolution based on the previously adduced reflux-impending mechanism.

scholarly journals Rare Case Report of Closed Traumatic Dislocation of Second to Fifth Metatarsophalangeal Joints

Cureus ◽  
2020 ◽  
Author(s):  
Santhosh Raj ◽  
Suresh Subramani ◽  
Suraj J Babar ◽  
Muthukumar S Balaji ◽  
Vijay Anand
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Traumatic Dislocation ◽  
Rare Case Report ◽  
Metatarsophalangeal Joints

scholarly journals A rare clinical case: schwannoma of tongue

2019 ◽  
Vol 5 (3) ◽  
pp. 789
Author(s):  
Chandra Veer Singh ◽  
Sheetal Radia ◽  
Saalim Sheikh ◽  
Vijay Haribhakti
Keyword(s):  
Head And Neck ◽  
Rare Case ◽  
Neck Region ◽  
Surgical Excision ◽  
Imaging Studies ◽  
Head And Neck Tumours ◽  
Head And Neck Region ◽  
Complete Surgical Excision ◽  
Slow Growing ◽  
Rule Out

<p class="abstract">Schwannoma are slow growing tumours, which can arise from any peripheral nerve. 10% of schwannomas that occur in the head and neck region mostly originate from the vagus or sympathetic nervous system. Extracranial schwannomas in the head and neck region are rare neoplasm. Intraoral schwannoma are only 1% of the all head and neck tumours. Diagnosis is established by imaging studies such as magnetic resonance imaging or computed tomography, while FNAC is used to rule out other conditions. We report a rare case of lingual schwannomas generally present as a painless lump schwannoma of the tongue in a 27-year-old male complaining of asymptomatic swelling over a posterolateral surface of the tongue, treated by complete surgical excision. The diagnosis was established on the basis of clinical, histopathological, and immunohistochemical examination. We report a rare case of schwannoma over the posterolateral surface of tongue. Prognosis is good for the patient when this condition is correctly diagnosed as the condition rarely recurs after complete resection.</p>

scholarly journals Managing traumatic testicular dislocations: what we know after two centuries

2020 ◽  
Vol 13 (11) ◽  
pp. e236801
Author(s):  
Sentilnathan Subramaniam ◽  
Muhammad Khairil Ab Khalil ◽  
Jasiah Zakaria ◽  
Firdaus Hayati
Keyword(s):  
Physical Examination ◽  
Motorcycle Accident ◽  
Surgical Reduction ◽  
Testicular Dysfunction ◽  
Inguinal Pain ◽  
Blunt Scrotal Trauma ◽  
Testicular Dislocation ◽  
Scrotal Trauma

Traumatic testicular dislocation (TTD) is a rare consequence of blunt scrotal trauma. A 21-year old gentleman presented with inguinal pain following a motorcycle accident and physical examination revealed absence of both testes within a well-formed scrotal sac with bilateral inguinal swellings. Ultrasonography confirmed viability and location of the testes at the superficial inguinal pouch. He underwent emergent surgical reduction with orchidopexy and was discharged the next day. No evidence of testicular dysfunction or atrophy was noted at follow-up. We reviewed reports of TTDs reported in English over the last two centuries and discuss its occurrence, evolution and management.

scholarly journals PAPILLARY CARCINOMA, A METASTASIS OF THE BRAIN AND BONE: A RARE CASE

2020 ◽  
Vol 73 (10) ◽  
pp. 2306-2308
Author(s):  
Volodymyr B. Dobrorodniy ◽  
Anatoliy D. Bedenyuk ◽  
Viktoria G. Khoperiia ◽  
Andriy V. Dobrorodniy
Keyword(s):  
Papillary Carcinoma ◽  
Rare Case ◽  
Cerebral Metastases ◽  
Papillary Thyroid ◽  
Rare Presentation ◽  
Large Size ◽  
Multiple Metastases ◽  
Uncommon Condition ◽  
Metastatic Sites ◽  
The Brain

Cerebral metastases from papillary carcinoma of the thyroid are a very uncommon condition. These metastases almost always involve concomitant lung or bone metastases which may be the first metastatic sites. In a 59-year-old woman found metastases of papillary thyroid cancer (PTC) in the frontal sinus, scapula, multiple bones of the skeleton and lungs. Evaluation confirmed that it is multiple metastases from PTC. This is a very rare presentation with such a large size of metastasis. We present this rare clinical case of massive distal lesions in PTC.

Rothia mucilaginosa: a case of septic arthritis in a native knee and review of the literature

2021 ◽  
Vol 14 (1) ◽  
pp. e237015
Author(s):  
Ahmed Daoub ◽  
Hamza Ansari ◽  
George Orfanos ◽  
Andrew Barnett
Keyword(s):  
Respiratory Tract ◽  
Septic Arthritis ◽  
Rare Case ◽  
Patient Management ◽  
Review Of The Literature ◽  
Gram Positive ◽  
Rothia Mucilaginosa ◽  
Uncommon Condition ◽  
Learning Points

Rothia mucilaginosa is a Gram-positive aerobic coccus usually found in the oral and respiratory tract. Septic arthritis is an uncommon condition, but is an orthopaedic emergency. A rare case of knee septic arthritis due to R. mucilaginosa is presented. Patient management and outcomes are discussed, and learning points from this case are outlined to help manage any further cases that may arise.

scholarly journals Leiomyosarcoma of the inguinal canal

2014 ◽  
Vol 96 (6) ◽  
pp. e8-e9 ◽  
Author(s):  
R Patel ◽  
P Chana ◽  
J Armstrong ◽  
R Lawrence
Keyword(s):  
Inguinal Hernia ◽  
Surgical Management ◽  
Rare Case ◽  
Inguinal Canal ◽  
Histological Findings

We describe a rare case of a leiomyosarcoma in the inguinal canal in a patient presenting clinically with an inguinal hernia. The clinical details, histological findings and surgical management are reviewed.

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