scholarly journals GASTROSCHISIS ASSOCIATED WITH COLONIC ATRESIA - CASE REPORT

2018 ◽  
pp. 81
Author(s):  
Ivona Đorđević ◽  
Anđelka Slavković ◽  
Zoran Marjanović ◽  
Dragoljub Živanović ◽  
Milan Petrović
Keyword(s):  
Case Report ◽  
Surgical Procedure ◽  
Rare Case ◽  
Colonic Anastomosis ◽  
Mechanical Obstruction ◽  
Postoperative Course ◽  
Colonic Atresia ◽  
Primary Surgery ◽  
Obstructive Ileus

We present an extremely rare case of gastroschisis associated with colonic atresia, anomaly seen in only 1.5-5% of all gastroschisis patients. Surgery for this anomaly can be very difficult due to the concomitant inflammation or other anomalies (mesenterium communae, volvulus, etc). Although prolonged intestinal dismotility is expected in these patients, mechanical obstruction must not be excluded in postoperative course, as it is explained in this case. Our case report demonstrates that primary colonic anastomosis is safe and well tolerated surgical procedure for these patients and that obstructive ileus is possible days after primary surgery and must not be overlooked.

scholarly journals Acquired colonic atresia in a 4-month old term male infant: a rare case report

2017 ◽  
Vol 4 (2) ◽  
pp. 669
Author(s):  
Kamal Nain Rattan ◽  
Gurupriya J. ◽  
Shruti Bansal ◽  
Rohit Kapoor ◽  
Roomi Yadav
Keyword(s):  
Case Report ◽  
Necrotizing Enterocolitis ◽  
Rare Case ◽  
Male Infant ◽  
Abdominal Distension ◽  
Exploratory Laparotomy ◽  
Inflammatory Mass ◽  
Colonic Atresia ◽  
Rare Case Report ◽  
History Of

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.

scholarly journals Liposarcoma Arising in the Foot: A Case Report

2009 ◽  
Vol 2009 ◽  
pp. 1-2 ◽  
Author(s):  
Toshihiro Matsuo ◽  
Takashi Sugita ◽  
Shoji Shimose ◽  
Tadahiko Kubo ◽  
Yuji Yasunaga ◽  
...  
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Soft Tissue Sarcoma ◽  
Rare Case ◽  
Lower Extremities ◽  
Postoperative Course ◽  
Rare Case Report ◽  
Low Incidence ◽  
Well Differentiated ◽  
Ray Amputation

Liposarcoma is categorized as a soft tissue sarcoma and most commonly appears in the lower extremities and rarely in the foot during adulthood. We present a very rare case report of a primary well-differentiated liposarcoma arising in the foot on a 60-year-old female. Marginal resection of the tumor with metatarsal ray amputation was eventually performed. The patient's postoperative course was uneventful without recurrence 5 years after the original operation. The authors review the literature and also report on the low incidence of this tumor arising in the foot.

Autogenous calcaneal bone graft repair of a closing base wedge osteotomy nonunion

1996 ◽  
Vol 86 (1) ◽  
pp. 25-32 ◽  
Author(s):  
J Pontious ◽  
JT Marcoux
Keyword(s):  
Case Report ◽  
Bone Graft ◽  
Surgical Procedure ◽  
Clinical Presentation ◽  
Wedge Osteotomy ◽  
Postoperative Course ◽  
First Metatarsal

The authors present a case report showing successful autogenous calcaneal bone graft stabilization of a first metatarsal closing base wedge osteotomy nonunion. The authors discuss the complications and clinical sequelae associated with first metatarsal base wedge osteotomy nonunions. The patient's clinical presentation, surgical procedure, and postoperative course are discussed. Comparative preoperative and postoperative objective gait analyses are presented. This approach to first metatarsal nonunion salvage appears to be clinically successful with a 15-month follow-up period.

scholarly journals DYSPLASTIC SPONDYLOLISTHESIS OF LUMBAR VERTEBRAE. A CASE REPORT

2005 ◽  
pp. 093-096
Author(s):  
Mikhail Vitalyevich Mikhailovsky ◽  
Aleksandr Vjacheslavovich Gladkov
Keyword(s):  
Case Report ◽  
Surgical Procedure ◽  
Rare Case ◽  
Iliac Crest ◽  
Lumbar Vertebrae ◽  
Deformation Pattern ◽  
Dorsal Spondylodesis

The paper reports a rare case of dysplastic multilevel spondylolisthesis of lumbar vertebrae in the girl of 15 years old followed up during 7 years. The deformation pattern and its progression have lead to a necessity of palliative surgical procedure of dorsal spondylodesis with autografts from the wing of iliac crest.

scholarly journals A Case of Two Abdominal Gossypibomas in a Patient: A Rare Case Report

2021 ◽  
Author(s):  
Radhika Batra ◽  
Richa Gautam ◽  
Alpana Manchanda ◽  
Deepak Ghuliani
Keyword(s):  
Computed Tomography ◽  
Case Report ◽  
Foreign Body ◽  
Caesarean Section ◽  
Surgical Procedure ◽  
Rare Case ◽  
Rare Condition ◽  
Lower Abdomen ◽  
Surgical Sponge ◽  
Rare Case Report

AbstractGossypiboma is a rare condition caused by retention of a foreign body, most commonly surgical sponge following any surgical procedure. The patient may be asymptomatic, can present with vague symptoms, or rarely with acute symptoms depending on the location of the foreign body and the complications associated with it; thus it may be difficult to diagnose this condition. A 30-year-old woman presented to our hospital with complaints of lump and mild pain on both sides of the lower abdomen for 3 months following caesarean section which was performed in a rural hospital. Ultrasound and computed tomography findings along with the classical history helped in arriving at the diagnosis of two gossypibomas in lower abdomen, one in each flank which was further confirmed on laparotomy.

Large Vulvar Lipoma in an Adolescent: A Case Report

JMS SKIMS ◽  
2011 ◽  
Vol 14 (1) ◽  
pp. 28-29
Author(s):  
R K Maurya ◽  
Pawan Kumar Singh ◽  
Sandeep Singh
Keyword(s):  
Case Report ◽  
Epithelial Cell ◽  
Adolescent Girl ◽  
Rare Case ◽  
Mesenchymal Cell ◽  
Benign Tumors ◽  
Melanocytic Tumors

Lipomas of vulva have been reported only rarely. Benign tumors of the vulva are normally classified according to their origin as epithelial cell tumors (e.g., keratinocytic, adnexal and ectopic tumors), or mesenchymal cell tumors (e.g., vascular, fibrous, muscular, neural, adipose and melanocytic tumors). Vulvar lipomas need to be differentiated from liposarcomas, which are rare but are very similar to lipomas clinically. Here we present a rare case of large vulvar lipoma in an adolescent girl. JMS 2011;14(1):28-29

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report

Empyema due to salmonella typhi in a diabetic patient: a rare case report

2011 ◽  
Vol 3 (6) ◽  
pp. 405-406
Author(s):  
Dr. Nale Swati S Dr. Nale Swati S ◽  
◽  
Dr.Ghadage Dnyaneshwari P ◽  
Bhore Arvind V
Keyword(s):  
Case Report ◽  
Diabetic Patient ◽  
Rare Case ◽  
Salmonella Typhi ◽  
Rare Case Report
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