scholarly journals 11-year-old female presenting with intermittent abdominal pain

2021 ◽  
Author(s):  
Fatema Ali ◽  
Jamie Lee ◽  
Kristen Cares
Keyword(s):  
Abdominal Pain ◽  
Intermittent Abdominal Pain

An Infant with COVID-19-Associated Intussusception

2021 ◽  
pp. 000313482110474
Author(s):  
Gwyneth A. Sullivan ◽  
Nicholas J. Skertich ◽  
Kody B. Jones ◽  
Michael Williams ◽  
Brian C. Gulack ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Abdominal Pain ◽  
Lymphoid Hyperplasia ◽  
Computed Tomography Scan ◽  
Ileocolic Intussusception ◽  
Common Cause ◽  
Caregiver Education ◽  
Intermittent Abdominal Pain ◽  
The Right ◽  
Tomography Scan

Intussusception is the most common cause of bowel obstruction in infants four to ten months old and is commonly idiopathic or attributed to lymphoid hyperplasia. Our patient was a 7-month-old male who presented with two weeks of intermittent abdominal pain associated with crying, fist clenching and grimacing. Ultrasound demonstrated an ileocolic intussusception in the right abdomen. Symptoms resolved after contrast enemas, and he was discharged home. He re-presented similarly the next day and was found to be COVID-19 positive. Computed tomography scan demonstrated a left upper quadrant ileal-ileal intussusception. His symptoms spontaneously resolved, and he was discharged home. This suggests that COVID-19 may be a cause of intussusception in infants, and infants presenting with intussusception should be screened for this virus. Additionally, recurrence may happen days later at different intestinal locations. Caregiver education upon discharge is key to monitor for recurrence and need to return.

scholarly journals Jejunojejunal intussusception secondary to submucosal lipoma resulting in a 5-year history of intermittent abdominal pain

2014 ◽  
Vol 2014 (oct29 1) ◽  
pp. bcr2014207297-bcr2014207297 ◽  
Author(s):  
I. Seow-En ◽  
F. J. Foo ◽  
C. L. Tang
Keyword(s):  
Abdominal Pain ◽  
Intermittent Abdominal Pain ◽  
History Of

A 48-year-old woman with a 4-month history of intermittent abdominal pain and urinary frequency

2014 ◽  
pp. 274-277
Author(s):  
Kirk J. Matthews ◽  
Jori S. Carter ◽  
David Chelmow ◽  
Christine R. Isaacs ◽  
Ashley Carroll
Keyword(s):  
Abdominal Pain ◽  
Urinary Frequency ◽  
Intermittent Abdominal Pain ◽  
History Of

scholarly journals A case report of mesenteric panniculitis

2019 ◽  
Vol 47 (7) ◽  
pp. 3354-3359 ◽  
Author(s):  
Ming-en Zhao ◽  
Ling-qiang Zhang ◽  
Li Ren ◽  
Zhen-wei Li ◽  
Xiao-lei Xu ◽  
...  
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Inflammatory Markers ◽  
Imaging Findings ◽  
Mesenteric Panniculitis ◽  
Intermittent Abdominal Pain ◽  
Rule Out

A 65-year-old man had intermittent abdominal pain for the previous 2 years. This pain suddenly became worse with a fever and elevated inflammatory markers. We took a while to diagnose the patient with mesenteric panniculitis (MP). Although imaging findings suggested MP, we needed to rule out other diseases. Choosing a treatment for the patient also took some time and we finally used glucocorticoid to cure the patient.

scholarly journals An atypical case of ectopic ACTH syndrome in an adolescent boy

2020 ◽  
Vol 2020 (3) ◽  
Author(s):  
Shreya Sharma ◽  
Rajesh Joshi
Keyword(s):  
Abdominal Pain ◽  
Adrenocorticotropic Hormone ◽  
Neuroendocrine Tumours ◽  
Ectopic Acth Syndrome ◽  
Ectopic Acth ◽  
Atypical Case ◽  
Intermittent Abdominal Pain ◽  
Pancreatic Net ◽  
Pancreatic Neuroendocrine Tumours ◽  
Ectopic Adrenocorticotropic Hormone

Abstract Ectopic adrenocorticotropic hormone (ACTH) syndrome (EAS) is exceedingly rare in children and scarcely reported. Pancreatic neuroendocrine tumours (NETs) can rarely lead to secretion of ectopic ACTH. A 14-year-old boy presented with hyperpigmentation, hypertension and intermittent abdominal pain, and was diagnosed with endogenous hypercortisolism. An incidental pancreatic mass discovered on routine ultrasonogram (USG) revealed the source of ACTH. He underwent successful excision of the mass with resolution of hypercortisolism. The histopathology revealed a Pancreatic NET and immunohistochemistry was positive for ACTH stain.

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