A Rare Case of Intra Mesenteric Dermoid Cyst

2021 ◽  
Vol 8 (05) ◽  
pp. 275-277
Author(s):  
Vikas Katiar ◽  
Kumar Vineet ◽  
Himanshu Singh ◽  
Sanjay Tripathi ◽  
Vikas Patel
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Female Patient ◽  
Rare Case ◽  
Rare Condition ◽  
Epidermal Cells ◽  
Mild Pain ◽  
Glandular Cells

A dermoid cyst is a teratoma of a cystic nature which can occur wherever a teratoma can occur. Intra mesenteric dermoid cyst is rarest of rare case and even its incidence is not known. Here, we report a case of intra mesenteric dermoid cyst in 21 yr. old female patient who presented to us with complain of on & off mild pain in abdomen for last 2 years. Intra mesenteric dermoid cyst is a rare condition and when presented with symptoms, it should be operated upon for improving patient’s overall wellbeing. Dermoids belong to the group of congenital cystic tumours developing from an embryonic rest. Such tumours vary from those which contain only epidermal cells to those containing various dermal derivatives, such as glandular cells (sebaceous), and even hair and teeth. So, they vary from pure epidermoids to dermoids and then through the teratoid tumours to the teratomas. These tumours can arise wherever two ectodermal surfaces fuse together in the developing embryo when an ectodermal implant is retained deep in the surface.”1 Intra mesenteric dermoid is very rare and no previous case report regarding intra mesenteric dermoid was found.

scholarly journals A Rare Case of Vaginal Dermoid Cyst: A Case Report and Review of Literature

2012 ◽  
Vol 3 (3) ◽  
pp. 102-104 ◽  
Author(s):  
Richa Sharma ◽  
Shashikala Nagraj
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Rare Case ◽  
Rare Condition ◽  
Review Of Literature ◽  
Transvaginal Approach ◽  
Investigative Tool

ABSTRACT Vaginal dermoid cyst is a rare condition. Ultrasound is the investigative tool and treatment is surgical through a transvaginal approach. How to cite this article Sharma R, Rao KA, Nagraj S. A Rare Case of Vaginal Dermoid Cyst: A Case Report and Review of Literature. Int J Infertility Fetal Med 2012;3(3):102-104.

scholarly journals Unilateral Acquired Posterior Maxillary Mandibular Syngnathia

2016 ◽  
Vol 24 (3) ◽  
pp. 161-165
Author(s):  
Abhishek Vijay Sahu ◽  
Kamalika Purkayastha Roy ◽  
Niva Kashyap
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Myositis Ossificans ◽  
Case Series ◽  
Rare Condition ◽  
International Literature ◽  
Bony Fusion ◽  
Maxilla And Mandible ◽  
Bony Ankylosis

Introduction: Congenital bony fusion of the maxilla and mandible, especially as an isolated occurrence, is a rare condition while acquired fusion being even rarer. Case report: A rare case of a 32 year old female patient with acquired unilateral bony fusion between the zygomatic arch of maxilla and ramus of mandible is reported. Discussion: Forty one cases of syngnathia has been reported in the international literature from 1936 to 2009, of which 39 cases are congenital and two were acquired, case 1 probably as a result of a fibrotic tubed pedicle and in case 2 from myositis ossificans. According to several case series, bony ankylosis of the mandible and maxilla has also been found to occur in 30%-43% of cases of NOMA.

scholarly journals A rare case of eight multiple primary malignant neoplasms in a female patient: A case report and review of the literature

2014 ◽  
Vol 9 (2) ◽  
pp. 587-590 ◽  
Author(s):  
JIEMIN ZHAO ◽  
YAN TAN ◽  
YUGANG WU ◽  
WEI ZHAO ◽  
JUN WU ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Case ◽  
Malignant Neoplasms ◽  
Review Of The Literature ◽  
Multiple Primary

scholarly journals A Case Report of Primary Pulmonary Choriocarcinoma in a Man: Successful Combination of Surgery and Chemotherapy

2020 ◽  
Vol 13 (2) ◽  
pp. 923-928
Author(s):  
Hang Thi Thuy Nguyen ◽  
Hung Huy Hoang ◽  
Anh Thi Van Le
Keyword(s):  
Case Report ◽  
Adjuvant Chemotherapy ◽  
Malignant Tumor ◽  
Rare Case ◽  
Rare Condition ◽  
Optimal Treatment ◽  
Reproductive Age ◽  
Women Of Reproductive Age ◽  
Standardized Treatment

Choriocarcinoma is a malignant tumor that typically appears in gonadal organs and primarily occurs in women of reproductive age. Being a primary extragonadal choriocarcinoma, primary pulmonary choriocarcinoma (PPC) is an extremely rare condition. Due to the rarity of PPC, no standardized treatment has been established so far. However, surgery combined with adjuvant chemotherapy appears to be the most optimal treatment. Here, we report a rare case of a man with PPC that was successfully treated with surgery followed by chemotherapy.

Intra Osseous Dermoid Cyst in Maxilla: A Rare Case Report

2015 ◽  
Vol 119 (3) ◽  
pp. e179
Author(s):  
Yeşim Yıldız ◽  
Burcu Sengüven ◽  
Sevil Kahraman ◽  
Benay Yıldırım
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Natal and Neonatal Teeth: A Case Report and Mecanistical Perspective

Healthcare ◽  
2020 ◽  
Vol 8 (4) ◽  
pp. 539
Author(s):  
Emil Anton ◽  
Bogdan Doroftei ◽  
Delia Grab ◽  
Norina Forna ◽  
Mihoko Tomida ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Condition ◽  
Radiographic Examination ◽  
Adequate Treatment ◽  
Dental Papilla ◽  
Ongoing Development ◽  
Risk Of Aspiration ◽  
The Relationship ◽  
Dental Papilla Cells

The presence of teeth on babies earlier than four months is a rare condition. Therefore, adequate treatment for each case should be instituted as soon as possible, considering that certain complications may arise. This report describes a rare case in which a newborn baby required the extraction of two mobile mandibular natal teeth to prevent the risk of aspiration. After two years, the clinical re-evaluation showed a residual tooth instead of a temporary one. This case report shows that adequate diagnosis should include a radiographic examination to determine whether these teeth are components of normal or supernumerary dentition, as well as further investigations on the relationship with the adjacent teeth. Another important aspect highlighted in this case report is the need for a post-extraction curettage of the socket in order to reduce the risk of ongoing development of the dental papilla cells.

scholarly journals Fetus papyraceus: a rare case report

2020 ◽  
Vol 7 (1) ◽  
pp. 113-116
Author(s):  
Namita Sindan ◽  
Adheesh Bhandari ◽  
Snigdha Rai ◽  
Devi Gurung
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Fetal Death ◽  
Rare Condition ◽  
Positive Outcome ◽  
Uterine Wall ◽  
Anatomical Location ◽  
Multiple Gestations ◽  
Gynecology And Obstetrics ◽  
Rare Case Report

Fetus papyraceus is a rare condition of a mummified and compressed fetus occurring in multiple gestations where one fetus dies in utero and is merged between the uterine wall and the membranes of living fetus. The blood vessels of the placenta of the two fetuses anastomose with each other, a third cycle occurs, causing fetal death (fetal transfer syndrome). Ultrasonography may identify the Fetus papyraceus, but is not always promising due to anatomical location. Cautious supervision is important during pregnancy for its positive outcome. We report a case of fetus papyraceus in Department of Gynecology and Obstetrics, Paropakar Maternity and Women’s Hospital, Kathmandu, Nepal.

Klippel-Feil Syndrome in Association with a Craniocervical Dermoid Cyst Presenting as Aseptic Meningitis in an Adult: Case Report

Neurosurgery ◽  
1989 ◽  
Vol 25 (4) ◽  
pp. 652-655 ◽  
Author(s):  
Bernadette Diekmann-Guiroy ◽  
Peter S. Huang
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Aseptic Meningitis ◽  
Rare Case ◽  
Craniocervical Junction ◽  
Spinal Tumors ◽  
Intracranial Tumors ◽  
Review Of The Literature ◽  
Adult Case

Abstract Intracranial tumors associated with Klippel-Feil syndrome usually occur in children, with spinal tumors being more common in adults affected by the syndrome. A rare case of a dermoid cyst at the craniocervical junction presenting as aseptic meningitis in an adult with Klippel-Feil syndrome is described. A review of the literature on tumors associated with this syndrome is also presented.

A rare case report of neonatal iliopsoas abscess presenting as swelling of left hip

2020 ◽  
pp. 1-6
Author(s):  
Maimoona Saeed ◽  
Iqtada Haider Shirazi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Clinical Presentation ◽  
Psoas Abscess ◽  
Rare Condition ◽  
Medical Sciences ◽  
Rare Case Report ◽  
Key Words Abscess ◽  
Systemic Antibiotics ◽  
Bluish Discoloration

Abstract We report the case of a 12 days old baby boy who presented with swelling and bluish discoloration on his left hip at Pakistan Institute of Medical Sciences in November 2018. Ultrasound (USS) was useful in making the diagnosis of a neonatal psoas abscess. He was treated with extraperitoneal drainage and with systemic antibiotics. The clinical presentation and diagnosis, treatment of this rare condition and brief literature review is given in this case report. Key Words: Abscess, Iliopsoas, Neonate, Staphylococcus aureus, Extraperitoneal Drainage. Continuous....

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