scholarly journals Complete Appendiceal Intussusception induced by Primary Adenocarcinoma of the Vermiform Appendix: A Rare Case Report and Review of the Relevant Literature

Author(s):  
Saptarshi Biswas ◽  
Samer Ebaid ◽  
Prem Patel

ABSTRACT Appendicular intussusception is a rare entity. Although first reported in 1858 there are only 250 cases reported since. In a large autopsy series the incidence rate of only 0.01% was documented. The exact pathophysiology is unclear but several etiologies have been documented. Primary adenocarcinoma of the appendix is extremely uncommon, which in most cases arises from a pre-existing adenoma. The incidence according to a reported study was documented as 0.08%. We report an uncommon case of a young female who presented with a 2-day history of abdominal pain with nausea and vomiting. Computed tomography scan suggested of ileocolic intussusception. Diagnostic laparoscopy was performed followed by open laparotomy. An appendicular tumor confirmed as adenocarcinoma of the appendix on frozen section was noted to be the cause of the intussusception. A right hemicolectomy was performed. We discuss the different anatomical and pathological factors causing appendicular intussusception with special emphasis on primary adenocarcinoma of the appendix, clinical features, classifications, preoperative diagnoses and treatment options of this rare disease entity along with review of relevant literature. How to cite this article Ebaid S, Biswas S, Patel P. Complete Appendiceal Intussusception induced by Primary Adenocarcinoma of the Vermiform Appendix: A Rare Case Report and Review of the Relevant Literature. Panam J Trauma Crit Care Emerg Surg 2015;4(1):36-38.

2014 ◽  
Vol 35 (5) ◽  
pp. 536-537 ◽  
Author(s):  
K. Chatzistamatiou ◽  
P. Tanimanidis ◽  
P. Xirou ◽  
F. Patakiouta ◽  
K. Kaplanis

2020 ◽  
Vol 7 (7) ◽  
pp. 1634
Author(s):  
Priyanka Sharma ◽  
Nishant Acharya ◽  
Trilok C. Guleria

Precocious puberty is defined as children attaining puberty more than 2.5 to 3 standard deviations (SD) earlier than the median age, or before the age of eight years in girls and nine years in boys. Hypothalamic hamartoma (HH) are rare, non progressive tumor like malformation. Precocious puberty due to HH occurs particularly at early ages, even 2 or 3 years. Treatment options for isolated CPP due to HH include GnRH analogs agonists continuously stimulates pituitary gonadotrophs, which further help in decreasing and desensitizing the release of LH, and to a lesser extent, FSH till the time puberty naturally set in. We present a case of precocious puberty due to hypothalamic hamartoma in 3 years old girl. Treated with GnRH analog lupirode and responded well to treatment with cessation of menstruation and reduction in breast size.


2013 ◽  
Vol 32 (02) ◽  
pp. 125-129
Author(s):  
Tiago de Paiva Cavalcante ◽  
Siegfried Pimenta Kuehnitzsch ◽  
George Santos dos Passos ◽  
José Eduardo Souza Dias Júnior ◽  
Tobias Engel Ayer Botrel ◽  
...  

AbstractThe PNET of CNS are considered malignant undifferentiated tumors, and it represents about 2,8% of all tumors found on infants and teenagers, more rarely found on adults. In the present article will report the case of a patient, male, 23 years-old, with nodular lesion inside the third ventricle, admitted on emergency room with acute intense headache, drowsiness, vomiting and visual clouding, started three days before. Although there have been advances in diagnosis and treatment of PNET in children, few publications were found on the efficiency of available treatment options on adults. In our patient the lesion was completely removed by a anterosuperior interhemispheric transcallosal craniotomy, and subsequently diagnosed as PNET by anatomopathological. Postoperative hydrocephaly was installed and reverted with a ventriculoperitoneal shunt, with clinical and neurological status improvement. The patient died 18 months after diagnosis, due to respiratory hospitalar infection.


2012 ◽  
Vol 2012 ◽  
pp. 1-3 ◽  
Author(s):  
Stefanos Atmatzidis ◽  
Grigoris Chatzimavroudis ◽  
Aristidis Patsas ◽  
Basilis Papaziogas ◽  
Spiros Kapoulas ◽  
...  

Colonic lipomas are uncommon nonepithelial neoplasms that are typically sessile, asymptomatic and incidentally found during endoscopy, surgery, or autopsy. We present a very rare case of a 34-year-old female patient with symptomatic pedunculated cecal lipoma causing intermittent colo-colonic intussusception. Despite adequate imaging studies, definite preoperative diagnosis was not established and the patient underwent exploratory laparotomy. Intraoperatively, intussusception of the cecum into the ascending colon was found and right hemicolectomy was performed. Macroscopic assessment of the resected specimen showed the presence of a giant cecal pedunculated polypoid tumor with features of lipoma, causing intussusception. Histopathological examination confirmed the diagnosis of pedunculated cecal lipoma.


2017 ◽  
Vol 7 (1) ◽  
pp. 64-67
Author(s):  
Mousumi Ahmed ◽  
Nazma Afroze ◽  
AJE Nahar Rahman ◽  
Mahjabin Sabiha

A bezoar is the result of the ingestion of indigestible or poorly digestible substances that accumulate in the gastrointestinal tract in the form of a mass. Among different types of bezoars phytobezoars is the most common type and formed by excessive consumption of herbal nutrients containing high amounts of indigestible fibers. There are some predisposing factors for gastrointestinal phytobezoars formation such as loss of pyloric function, decreased gastric motility, malabsorption, inadequate chewing and excessive consumption of herbal indigestible fibers. Small bowel obstruction is the most common major complication of phytobezoars. We present a rare case of intestinal obstruction in a middle aged man who was previously diagnosed to have malabsorption and used to take herbal medicine. He was treated successfully by right hemicolectomy under general anesthesia. On histopathological examination a large phytobezoar was found in the terminal part of ileum.Birdem Med J 2017; 7(1): 64-67


2021 ◽  
Author(s):  
Kaiping Zhang ◽  
Ye Zhang ◽  
Yin Zhang ◽  
Min Chao

Abstract Background: Testicular hemangioma is a extremely rare and typically occurs in childhood or adolescence. It is a benign tumor that appears as a slowly growing painless mass.Case presentation: We herein present the case of a 3 year-old male patient with testicular hemangioma accompanying hydrocele, who underwent surgical resection.Conclusions: This article discusses the diagnosis and currently available treatment options of testicular hemangioma. It also can be provide clinical experiences for urologist in face of similar situation.


2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko

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