A Giant Intradiaphragmatic Bronchogenic Cyst: Case Report and Literature Review

2017 ◽  
Vol 103 (1_suppl) ◽  
pp. S25-S27 ◽  
Author(s):  
Xin Gao ◽  
Min Zhai ◽  
Haitao Zhang ◽  
Yunliang Wang ◽  
Jin Zhou
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Chest Pain ◽  
Literature Review ◽  
Bronchogenic Cyst ◽  
Early Embryogenesis ◽  
Congenital Lesions ◽  
Left Diaphragm ◽  
The Right ◽  
Bronchogenic Cysts

Bronchogenic cysts are congenital lesions developing during early embryogenesis. The intradiaphragmatic location is extremely rare. We present a giant bronchogenic cyst arising from the left crus of diaphragm. Based on our literature review results, intradiaphragmatic bronchogenic cysts have the following characteristics: 1) they are more common in female patients; 2) the patients are usually asymptomatic, or present with symptoms of chest pain, abdominal pain, and hiccups; 3) the cysts located in the left diaphragm are more than those in the right diaphragm, most of which are located in the area of the left diaphragm crus.

scholarly journals Duplicate Vas Deferens Encountered during Inguinal Hernia Repair: A Case Report and Literature Review

2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Maxwell C. Breitinger ◽  
Evan H. Roszkowski ◽  
Adam J. Bauermeister ◽  
Andrew A. Rosenthal
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Inguinal Hernia ◽  
Literature Review ◽  
Hernia Repair ◽  
Spermatic Cord ◽  
Doppler Ultrasonography ◽  
Vas Deferens ◽  
Incarcerated Inguinal Hernia ◽  
The Right

Duplication of the vas deferens is a rare anomaly, defined as the presence of two distinct vasa deferentia within one spermatic cord, with only 28 cases reported worldwide since 1959. We report the case of a 63-year-old man with a duplicate vas deferens, presenting with abdominal pain from bowel obstruction secondary to incarcerated inguinal hernia. Spermatic cord dissection during hernioplasty revealed duplication of the vas deferens within the right spermatic cord. Doppler ultrasonography confirmed absence of waveforms in both vasa deferentia with arterial signal in the accompanying vessel. The hernia was repaired without complication. This report emphasizes recognition of duplicate vas deferens in avoiding iatrogenic injury and optimizing surgical outcome.

scholarly journals Lipoma-Like Bronchogenic Cyst in the Right Chest Sidewall: A Case Report and Literature Review

2016 ◽  
Vol 22 (6) ◽  
pp. 370-374 ◽  
Author(s):  
Wen-cheng Che ◽  
Qi Zang ◽  
Qiang Zhu ◽  
Tian-chang Zhen ◽  
Gong-zhang Su ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Bronchogenic Cyst ◽  
The Right

Needle fragment embolism into the right ventricle: a rare cause of chest pain case report and literature review

2015 ◽  
Vol 128 (5-6) ◽  
pp. 215-220 ◽  
Author(s):  
Barbara Anna Danek ◽  
Petr Kuchynka ◽  
Tomas Palecek ◽  
Vladimir Cerny ◽  
Karel Hlavacek ◽  
...  
Keyword(s):  
Case Report ◽  
Chest Pain ◽  
Literature Review ◽  
Right Ventricle ◽  
The Right

scholarly journals Rupture and hemorrhage of a seminoma mixed with yolk sac tumors in 46XY partial gonadal dysgenesis: a case report and literature review

BMC Surgery ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Rui Lin ◽  
Nanbin Liu ◽  
Xiuyan Wang ◽  
Xuyou Zhu ◽  
Daojing Huang ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Literature Review ◽  
Germ Cell ◽  
Gonadal Dysgenesis ◽  
Yolk Sac ◽  
Sex Development ◽  
Yolk Sac Tumors ◽  
Partial Gonadal Dysgenesis ◽  
The Right

Abstract Background 46XY partial gonadal dysgenesis (PGD) is a rare subtype of disorder of sex development (DSD). 46YY PGD is a congenital disease with atypical chromosomal, gonadal, or anatomical sex development. The patient in this case report had male and female genitalia simultaneously. We created a flowchart of the differential diagnosis for clinicians. Case presentation A 41-year-old male was admitted to the hospital complaining of lower quadrant abdominal pain for 1 day. Physical examination revealed that his penis size was normal, but a urethral orifice was located in the perineum area between the scrotum and anus. One small testicle was in the left scrotum, but no testicle was present on the right. The patient’s abdomen was bulging, and he had lower abdominal pain. According to the emergency CT scan, a lesion (74*65 mm) was found in the right pelvis between the bladder and rectum. The lesion showed an unclear boundary and hematocele appearance. The lesion was removed by emergency surgery, and the pathology report indicated a mixed germ cell tumor with a seminoma and yolk sac tumors. Conclusion This article is a case report of germ cell tumors in 46XY PGD patients. The literature review summarizes the clinical diagnosis, and a flowchart is provided for physicians in future practice. The importance of this report is that it will help acquaint physicians with this rare disease and make the right initial clinical decision quickly through the use of this flowchart. However, the variants of special subtypes of 46XY DSD are myriad, and all the diagnoses could not be covered in one flowchart.

Recurrent neck abscess due to a bronchogenic cyst in an adult

2010 ◽  
Vol 124 (12) ◽  
pp. 1325-1328 ◽  
Author(s):  
A J C Hazenberg ◽  
L M Pullmann ◽  
R-P Henke ◽  
F Hoppe
Keyword(s):  
Case Report ◽  
Bronchogenic Cyst ◽  
Radiological Imaging ◽  
Neck Abscess ◽  
Aged Woman ◽  
Middle Aged Woman ◽  
Deep Neck Abscess ◽  
The Right ◽  
Cervical Cysts ◽  
Bronchogenic Cysts

AbstractBackground:Neck abscesses can originate from congenital cervical cysts. Cervical cysts of bronchogenic origin are rare and often asymptomatic. Common symptoms of bronchogenic cysts are stridor, dyspnoea and dysphagia. The reported patient represents the second published case of a bronchogenic cyst causing a neck abscess in an adult.Case report:We report a case of a cervical bronchogenic cyst presenting as a recurrent supraclavicular abscess in a middle-aged woman. During extirpation, a fistula was demonstrated to the right upper lobe of the lung, suspected because the cyst inflated synchronously with respiration.Discussion:The symptoms of bronchogenic cysts are due to the effects of compression or fistulas. In the majority of these cysts, a thorough investigation involving history, examination and radiological imaging does not clearly demonstrate a fistula. Therefore, extirpation is both diagnostic and therapeutic.Conclusion:A bronchogenic cyst is a very rare cause of a recurrent deep neck abscess. Total extirpation is the treatment of choice.

scholarly journals Retroperitoneal Bronchogenic Cyst Mimicking Hydatid Liver: A Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-2
Author(s):  
Fazl Q. Parray ◽  
Afak Yusuf Sherwani ◽  
Sajad Ahmad Dangroo ◽  
Rafia Aziz Bisati ◽  
Nighat Shaffi Malik
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Bronchogenic Cyst ◽  
Hydatid Cysts ◽  
Retroperitoneal Bronchogenic Cyst ◽  
The Right ◽  
Bronchogenic Cysts

Bronchogenic cysts frequently occur in the mediastinum. They may be rarely encountered in the abdomen and retroperitoneum. Bronchogenic cysts can in fact mimic hydatid cysts. We report a case of retroperitoneal bronchogenic cyst below the right hemidiaphragm mimicking a hydatid cyst of the liver in a 30-year-old female.

scholarly journals How to Approach to Torsional Adnexal Mass in a Geriatric Age Woman: A Case Report and Literature Review

2019 ◽  
Vol 4 (09) ◽  
Author(s):  
Recep ERİN ◽  
Yeşim BAYOĞLU TEKİN ◽  
Fatma Gülgün KOÇAK
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Literature Review ◽  
Adnexal Mass ◽  
Complete Recovery ◽  
Total Abdominal Hysterectomy ◽  
Abdominal Hysterectomy ◽  
Adnexal Torsion ◽  
Gynecologic Emergency ◽  
The Right

We aimed to present how to approach to the postmenopausal torsional adnexal masses, accompanied by a case report and literature review. A 90 year-old geriatric age woman with G5P5 admitted to emergency department with complaints of nausea, vomiting and abdominal pain. We detected a tumoral mass with solid component and irregular surface suspected malignancy in the midline of the pelvis. Laparotomy was performed due to the suspicion of torsion and malignancy. We detected a approximately 25 cm torsional blue-purple colored tumoral mass originating from the right ovary and performed total abdominal hysterectomy and bilateral salpingo-oferectomy. Pathology was reported as a sex cord stromal tumor with torsional. The patient was discharged with complete recovery on the 3rd postoperative day. Adnexal torsion is a gynecologic emergency. It should be considered in postmenopausal women who present with abdominal pain and adnexal mass.

scholarly journals Appendicular endometriosis as a cause of chronic abdominal pain alone in the right iliac fossa: case report and literature review

2012 ◽  
Vol 32 (1) ◽  
pp. 79-82
Author(s):  
Marcelo Pandolfi Basso ◽  
Adriana Borgonovi Christiano ◽  
André Luís Cozetto de Oliveira ◽  
Geni Satomi Cunrath ◽  
João Gomes Netinho
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Literature Review ◽  
Iliac Fossa ◽  
Chronic Abdominal Pain ◽  
The Right

Popliteal nodal metastasis from squamous cell cancer of the foot. Case report and literature review

2019 ◽  
pp. 1-2
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Literature Review ◽  
Squamous Cell ◽  
Rare Case ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Nodal Metastasis ◽  
Regional Disease ◽  
The Right

We report a very rare case of squamous cell cancer of the right foot which had metastasize to the ipsilateral popliteal lymph node after initial diagnosis and treatment for the loco-regional disease.

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.

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