scholarly journals Mummified papyraceous fetuses in the abdominal cavity of an elderly female dog with pyometra

2012 ◽  
Vol 64 (2) ◽  
pp. 311-317 ◽  
Author(s):  
F.A. Voorwald ◽  
C.F. Tiosso ◽  
D.J. Cardilli ◽  
G.H. Toniollo

This paper reports on a rare case of fetal papyraceous mummification after asymptomatic uterine rupture in an elderly female dog with pyometra. The patient had a history of mating six months before the examination but no apparent signs of gestation or parturition. Exploratory laparotomy was used to identify a rupture of the left uterine horn and the presence of cystic endometrial hyperplasia and pyometra. Two mummified papyraceous fetuses were observed in the abdominal cavity and had adhered to the spleen, pancreas, intestine and omentum. Ovariehysterectomy and corrective surgery were performed. The patient had remained healthy after uterine rupture until a new estrous cycle and the development of pyometra. Bitches that are 10 years old or more are predisposed to implantation failure, pregnancy or parturition problems and they should not be breed to avoid complications.

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Hironori Yamashita ◽  
Yasuhiro Fujino ◽  
Tadayuki Ohara ◽  
Keitaro Kakinoki ◽  
Takemi Sugimoto ◽  
...  

Abstract Background Solitary fibrous tumor (SFT) is a rare mesenchymal tumor that typically arises from the pleura. Although it may appear in other organs, it rarely develops in the pancreas. We report herein a rare case of metastatic SFT of the pancreas originating from an intracranial tumor and subsequently identified as a cystic neoplasm of the pancreas. Case presentation A 58-year-old woman with a past medical history of brain tumor visited the hospital for further investigation of a cystic tumor in the pancreas tail. Abdominal imaging showed a heterogeneously enhancing mass that was initially suspected as a neuroendocrine neoplasm, solid pseudopapillary neoplasm, or mucinous cystic neoplasm of the pancreas. Distal pancreatectomy was performed without any intraoperative and postoperative complications. Pathological findings confirmed a diagnosis of malignant SFT of the pancreas with hyperproliferative potential. A histopathological review of her brain tumor revealed that the pancreatic tumor was derived from her brain lesion. The patient developed recurrent brain disease 4 years after the pancreatectomy, but no recurrence has been observed in the abdominal cavity. Conclusions SFT should be considered in the differential diagnosis of untypical hypervascular pancreatic mass, particularly in patients with a history of an intrathoracic or intracranial mesenchymal tumor. Immunohistochemical analysis is crucial in detecting this tumor entity. Hyperproliferative status indicates a malignant disease and requires careful postoperative observation.


2017 ◽  
Vol 2017 ◽  
pp. 1-4
Author(s):  
Beng Kwang Ng ◽  
Kembang Aziah Yakob ◽  
Wendy Yin Ling Ng ◽  
Pei Shan Lim ◽  
Rahana Abd Rahman ◽  
...  

Tuberculosis (TB) remained as one of the top 10 causes of death worldwide despite an overall decline in its incidence rate globally. Extrapulmonary TB is uncommon and only accounts for 10–20% of overall TB disease burden. Abdominopelvic TB is the sixth most common location of extrapulmonary TB. The symptoms and signs are often insidious and nonspecific. Diagnosing abdominopelvic TB can be very challenging at times and poses great difficulties to the clinician. Infection with nontuberculous Mycobacterium (NTM) is even rarer especially in an immunocompetent patient. We report a case of NTM in abdominopelvic TB. A 37-year-old foreign worker, para 3, presented with a one-week history of suprapubic pain associated with fever. An assessment showed presence of a right adnexal mass. She was treated as tuboovarian abscess with intravenous antibiotics. Unfortunately, she did not respond. She underwent exploratory laparotomy. Intraoperatively, features of the mass were suggestive of a right mature cystic teratoma with presence of slough and cheesy materials all over the abdominal cavity as well as presence of ascites. Diagnosis of NTM was confirmed with PCR testing using the peritoneal fluid. This case was a diagnostic dilemma due to the nonspecific clinical presentation. Management of such rare infection was revisited.


2017 ◽  
Vol 4 (2) ◽  
pp. 669
Author(s):  
Kamal Nain Rattan ◽  
Gurupriya J. ◽  
Shruti Bansal ◽  
Rohit Kapoor ◽  
Roomi Yadav

Acquired colonic atresias are very rare but, are known in association with necrotizing enterocolitis. We report a case of a 4-month term male infant with recurrent episodes of abdominal distension, bilious vomiting and constipation off and on, without the history of necrotizing enterocolitis. Exploratory laparotomy was performed, an inflammatory mass with multiple dense interloop adhesions were found in the mid-transverse colon. These adhesions were lysed to identify the proximal dilated and distal blind end of the colon.  Rest of the gut was normal.  This case is unique for the fact that, it is a case of acquired colonic atresia without history of necrotizing enterocolitis, unlike other reported cases of acquired colonic atresia.


2021 ◽  
Vol 156 (Supplement_1) ◽  
pp. S128-S129
Author(s):  
K Broder ◽  
R L Geller ◽  
C Del Rio ◽  
D Bhamidipati

Abstract Introduction/Objective Infection with Pneumocystis jirovecii remains a common cause of pneumonia in patients with Acquired Immune Deficiency Syndrome (AIDS). Extrapulmonary manifestations, however, are exceedingly rare. We describe a rare case of coinfection of the small bowel by Pneumocystis jirovecii and cytomegalovirus (CMV). Methods/Case Report A 48-year-old female with a history of HIV/AIDS, remote history of Pneumocystis jirovecii pneumonia, and previous non-compliance with HAART, presented to the emergency department with right lower quadrant abdominal pain, fever, and chills for 1 week. Her recent medical history included a hospital admission 1 month prior for community-acquired pneumonia with CD4 count and viral load of 12 cells/mcl and >680,000 copies/mL, respectively; upon discharge she restarted HAART. When she presented to the emergency department in our case, she demonstrated leukocytosis (14.3 K/mcl), tachycardia (131 bpm), and hypotension (87/58 mmHg). An abdominal CT scan showed free air with concern for perforated viscus and multi-station lymphadenopathy with gastrohepatic and retrocaval nodes >2 cm. A chest x-ray showed nodular and cavitary lesions, stable from prior imaging. The differential diagnoses in an AIDS patient with a gastrointestinal mass includes Kaposi’s sarcoma, lymphoproliferative process, or infection. The surgeons were concerned for tuberculosis as well, due to the hospital’s patient population, her bulky lymphadenopathy, and immune-compromised status. An exploratory laparotomy was performed and found jejunal perforations, mesenteric lymphadenopathy, and 3L of fluid in the abdomen. Pathology received 4 soft lymph nodes and a 57 cm segment of thickened small bowel with purulent perforation but no discrete mass. Microscopic examination showed a perforating pseudotumor and acute serositis extending to the margins of the specimen. Lymph node flow cytometry was negative for clonal populations. GMS stains highlighted innumerable “crushed-ping-pong-ball”-like fungal forms consistent with Pneumocystis in the jejunum and all 4 lymph nodes. A CMV immunohistochemical stain highlighted infected cells with nuclear enlargement and nuclear inclusions in the jejunum. Results (if a Case Study enter NA) NA Conclusion Extrapulmonary Pneumocystis infection is rare but clinicians, pathologists, and microbiologists must keep it in the differential of HIV patients, especially those who are not controlled on antiretroviral therapy.


Author(s):  
Durga K.

Uterine rupture in pregnancy is very rare and potentially catastrophic for both mother and foetus. The most common cause of uterine rupture is giving away of previous caesarean uterine scar. Spontaneous rupture of an unscarred uterus during pregnancy is a rare occurrence. We hereby present a rare case of a spontaneous complete uterine rupture in a non-labouring unscarred uterus of a 33-year-old nulliparous woman at 35 weeks of gestation. She presented with lower abdomen pain and decreased foetal movements at Institute of Obstetrics and Gynaecology, Chennai. Even before getting into labour, patient suddenly collapsed, and emergency laparotomy was proceeded in view of suspicious concealed abruption. There was frank hemoperitoneum along with a dead baby in the abdominal cavity. There was rupture of uterine fundus extending from one cornual end to the other and closure of uterine rent proceeded. Spontaneous rupture of uterus occurs when there is an upper segment uterine scar. She had a past history of eventful uterine curettage which was the risk factor for uterine rupture. 


2017 ◽  
Vol 4 (10) ◽  
pp. 3564
Author(s):  
Manish Bansal ◽  
Sameer Gupta ◽  
Kanika Goel ◽  
Sulbha Mittal

Gastrointestinal stromal tumours (GISTs) are mesenchymal tumors arising in the gastrointestinal tract (GIT).  In GIT, the most common site of presentation is stomach followed by small intestine, colon, rectum and oesophagus. Here we report a rare case of intraluminal jejunal GIST with history of pain abdomen, occasional vomiting and GI bleed. Patient was taken up for exploratory laparotomy. Intraoperative findings revealed a hard-nodular growth in antimesenteric border of jejunum, 5 cm distal to duodenojejunal flexure (DJ) partially obstructing the lumen. Anastomosis was quite difficult due to presence of growth near DJ flexure and chances of leak were high. The patient had an uneventful postoperative course and doing well after 1 year of follow up with no recurrence.


2019 ◽  
Vol 7 (1) ◽  
pp. 303
Author(s):  
Mezhuneituo Raleng ◽  
Anant Prakash Pore ◽  
Vickey Katheria ◽  
Worshim Khamrang ◽  
R. S. Wungramthing

A 70 year old male who was under treatment for lymphoma, presented with a 2 day old history of not passing stool, flatus, associated with vomiting and abdominal distension. Patient was diagnosed as subacute intestinal obstruction and put on conservative management. However since his condition worsen exploratory laparotomy was performed. On laparotomy a midgut volvulus was detected and subsequently de-rotation of small gut was done. Through this paper we would like to stress out the difficulties in diagnosis and the challenges that we faced. 


2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
George S. Karagiannis ◽  
Mihalis Pelekanis ◽  
Panayiotis Loukopoulos ◽  
Haris N. Ververidis ◽  
Eleni Kaldrymidou

An 11-year-old Labrador Retriever bitch with a history of intermittent, sanguineous vaginal discharge of a six-month duration was presented. During exploratory laparotomy, two well-delineated, intramural masses were identified bilaterally in the uterine horns. Histopathologic examination of the mass on the left horn showed that it was a typical leiomyoma. However, the second mass appeared with an unusual coexistence of histological lesions, involving epithelial tissue foci, mild focal adenomyosis, and cystic endometrial hyperplasia. Interestingly, such combination was never encountered before in dogs. Although uterine leiomyoma is quite usual in the reproductive system of female dogs, this case resembled relevant cases of human uterine adenomyomas in morphology, and thus it was offered a similar tentative diagnosis.


Author(s):  
Akshay vijay Yadav ◽  
Kamalakar Vasant Gajare

(1)Meckel’s diverticulum is the most common abnormality of the gastrointestinal tract. It is present in more than 2% of the global human population. (2)Haemorrhage, obstruction and inflammation are the three main possible complications resulting from Meckel’s diverticulum. Spontaneous perforation of Meckel’s diverticulum is very rare and may mimic acute appendicitis. We are reporting the case of a 22 year-old female patient, who presented with a history of five days of acute abdominal pain including on-and-off fever, emesis and vertigo. On physical examination, her abdomen was distended with guarding all over it. A provisional diagnosis of perforated appendicitis with peritonitis or intestinal perforation was made. So CT abdomen with contrast was done. It was reported as sealed perforation with diverticulitis. A diagnostic laparoscopy followed by exploratory laparotomy and subsequent resection and anastomosis of the ileum was performed under general anaesthesia. Meckel’s diverticulitis was confirmed by histopathological findings. This case report is an interesting and unusual case of complications associated with inflamed Meckel’s diverticulum and emphasizes the importance of considering Meckel’s diverticulitis as a differential diagnosis in every patient presenting with acute abdomen. Keywords:   Meckel’s diverticulum, appendicitis, peritonitis   


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