scholarly journals PURE YOLK CELL TESTICULAR TUMOR; A 23 YEAR OLD MALE PATIENT, A RARE ENTITY

2017 ◽  
Vol 24 (04) ◽  
pp. 637-638
Author(s):  
Muhammad Sheraz Javed ◽  
Muhammad Irfan Munir ◽  
Muhammad Saad Siddique
Keyword(s):  
Male Patient ◽  
Testicular Tumor ◽  
Rare Entity ◽  
Yolk Cell

Congenital Intercostal Hernia: A Rare Entity

JMS SKIMS ◽  
2018 ◽  
Vol 21 (1) ◽  
pp. 48
Author(s):  
Syed Muzamil Andrabi ◽  
Mohd Yousuf Dar ◽  
Javid Ahmad Bhat
Keyword(s):  
Male Patient ◽  
General Surgery ◽  
Rare Entity ◽  
Intercostal Hernia ◽  
History Of ◽  
Lateral Chest ◽  
Patient Department

A 35-year-old male patient presented to the General Surgery Out Patient Department with a history of swelling on the left lateral chest since birth. The swelling appeared during inspiration and disappeared during expiration. JMS 2018;21(1):48 

scholarly journals Raspberry-like tumor on the skin – A rare entity

2019 ◽  
Vol 1 ◽  
pp. 91-93
Author(s):  
Soumya Sreedharan ◽  
Kunjumani Sobhanakumari ◽  
Fousiya Pulikkal ◽  
Machiyanickel Issac Celine ◽  
Parapattu K. Balachandran
Keyword(s):  
Nasal Cavity ◽  
Male Patient ◽  
Rare Entity ◽  
Rhinosporidium Seeberi ◽  
Granulomatous Infection

Rhinosporidiosis is a chronic granulomatous infection, caused by Rhinosporidium seeberi, which frequently affects the nasal cavity and nasopharynx. Cutaneous rhinosporidiosis is rare and probably underreported. We report a case of cutaneous rhinosporidiosis in association with recurrent nasopharyngeal rhinosporidiosis in a 68-year-old male patient.

scholarly journals Rare case of solitary plasmacytoma of the skull in a young male patient

2017 ◽  
Vol 21 (1) ◽  
Author(s):  
Swati Singh ◽  
Vaishali Upadhyaya ◽  
Rajat Agarwal ◽  
Ratni B. Gujral
Keyword(s):  
Elderly Patient ◽  
Multiple Myeloma ◽  
Male Patient ◽  
Rare Case ◽  
Osteolytic Lesion ◽  
Young Male ◽  
Axial Skeleton ◽  
Solitary Plasmacytoma ◽  
Age Group ◽  
Rare Entity

Solitary plasmacytoma of bone without signs of multiple myeloma is a rare entity. It usually presents as an osteolytic lesion in the axial skeleton of an elderly patient. Here, we report a case of solitary plasmacytoma in the skull of a young male patient which emphasises the need to consider it in the differential diagnosis of a destructive calvarial mass lesion even in this age group.

scholarly journals Amyand’s hernia: acute appendicitis and abscess in the inguinal canal

2019 ◽  
Vol 12 (7) ◽  
pp. e228725
Author(s):  
Anna Junttila ◽  
Anne K Mattila
Keyword(s):  
Acute Appendicitis ◽  
Male Patient ◽  
Inguinal Canal ◽  
Amyand’S Hernia ◽  
Diagnostic Process ◽  
Rare Entity

Amyand’s hernia is a rare entity where the appendix is trapped within inguinal canal. For even rarer are the cases where the appendix has perforated and caused an abscess into inguinal canal. Here we report a case where a male patient had Amyand’s hernia, acute appendicitis and abscess which were treated by laparotomy. We present the diagnostic process and intraoperative finding leading to diagnosis of Amyand’s hernia.

Lipoma arboresecente de la grasa de hoffa. Reporte de caso y revisión del tema.

2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Giselle Fernández García ◽  
Luis Bastián Manso
Keyword(s):  
Knee Joint ◽  
Key Words ◽  
Male Patient ◽  
Synovial Membrane ◽  
Rare Entity ◽  
Fat Pad ◽  
Previous Trauma ◽  
The Right

The lipoma arborescent of the knee consists of a benign villonodular proliferation of fat under the synovial membrane. It is a rare entity often secondary to previous trauma. Hoffa's fat is an extrasynovial intracapsular fat pad that which looks like a quadrangular pyramid is in the anterior-inferior compartment of the knee joint. The case of a 44-year-old male patient is presented, professional trainer, who complains of pain and increased volume of the anterolateral region of the right knee. Arborescent lipoma of Hoffa's fat is diagnosed. Key words: lipoma arborescent, Hoffa fat, knee lipoma, benign Hoffa fat tumor

scholarly journals Strangulated lumber hernias in adults: A case report and review of the literature

2016 ◽  
Vol 98 (8) ◽  
pp. e160-e161 ◽  
Author(s):  
I Ka ◽  
ML Gueye ◽  
O Thiam ◽  
LG Akpo ◽  
AO Toure
Keyword(s):  
Case Report ◽  
Male Patient ◽  
Preoperative Diagnosis ◽  
Rare Condition ◽  
Lumbar Hernia ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Management Guideline ◽  
Therapeutic Modalities ◽  
Specific Management

Strangulated lumbar hernia is a very rare condition, with no more than 30 cases reported in the literature so far. Therefore, there is no specific management guideline and the diagnosis remains difficult. By reporting the case of a Senegalese male patient who had a preoperative diagnosis of strangulated lumbar hernia, we aim to discuss the diagnosis and therapeutic modalities of this rare entity, which is often misdiagnosed.

scholarly journals Sterile Neutrophilic Folliculitis with Vasculopathy in a Young Male Patient with Infective Endocarditis

2019 ◽  
Vol 3 (5) ◽  
pp. 362-365
Author(s):  
Carl Barrick ◽  
Emily Chea ◽  
Naeha Gupta ◽  
Richard McClain ◽  
Steven Purcell
Keyword(s):  
Infective Endocarditis ◽  
Clinical Features ◽  
Male Patient ◽  
Systemic Disease ◽  
Young Male ◽  
Clinical Entity ◽  
Cutaneous Manifestation ◽  
Diagnosis And Treatment ◽  
Medical Illness ◽  
Rare Entity

Sterile neutrophilic folliculitis with vasculopathy is a rare entity histopathologically characterized by neutrophilic or suppurative and granulomatous folliculitis accompanied by a folliculocentric vasculopathy.1 It is described as a cutaneous manifestation of a systemic illness or infectious trigger, and its clinical features vary independently from the underlying medical illness.1 Prompt identification may uncover an underlying systemic disease. Due to the rarity of this clinical entity, there is a paucity of evidence regarding its etiology, diagnosis, and treatment recommendations. We present a case of sterile neutrophilic folliculitis with vasculopathy in a 34-year-old male hospitalized for infective endocarditis.

scholarly journals Primary Hydatid of Adductor Muscle of Thigh: A Rare Entity

2019 ◽  
Vol 9 (1) ◽  
pp. 30-32
Author(s):  
Punyapratap Singh ◽  
Somshankar Pandey ◽  
Vrishbhan Ahirwar
Keyword(s):  
Soft Tissue ◽  
Male Patient ◽  
Hydatid Disease ◽  
Soft Tissue Tumor ◽  
Histopathological Examination ◽  
Adductor Muscle ◽  
Rare Entity ◽  
Imaging Studies ◽  
Muscle Involvement ◽  
Multiple Imaging

Primary Muscle involvement of hydatid disease is a rare entity. Radiological diagnosis can be difficult at times as it mimics soft tissue tumor. Multiple imaging studies are available to detect it preoperatively. We hereby report an in a male patient with hydatid disease of adductor group of muscles of right thigh diagnosed on ultrasound followed by MRI and confirmed on surgery and histopathological examination.

scholarly journals Rare cause of Bow Hunter’s syndrome due to an aberrant course of a vertebral artery

2019 ◽  
Vol 12 (7) ◽  
pp. e229584
Author(s):  
Kaishin Tanaka ◽  
Brendan Steinfort
Keyword(s):  
Vertebral Artery ◽  
Male Patient ◽  
Cervical Vertebrae ◽  
Distal Portion ◽  
Posterior Circulation ◽  
Left Vertebral Artery ◽  
Vertebrobasilar Insufficiency ◽  
Rare Entity ◽  
Hunter's Syndrome

Bow Hunter’s syndrome (BHS) is a rare cause of vertebrobasilar insufficiency and is reported to most commonly be caused by vertebral artery impingement on cervical vertebrae osteophytes. We report a case in a 56-year-old male patient who on investigation of recurrent posterior circulation ischaemic strokes was found to have BHS. The aetiology of the syndrome in this patient is due to a particularly unusual aberrancy in the path of the atlantoaxial portion of the culprit left vertebral artery. Aberrancy of the distal portion of the vertebral artery is in itself a rare entity, and there are few reports of it in relation to BHS. The patient in this case was successfully treated with endovascular sacrifice of the vertebral artery with no further dynamic occlusive symptoms.

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