Hi everyone!
I am trying to figure out a diagnosis for my son and I'm very frustrated. We've seen the pediatrician, the endocrinologist (for his failure to thrive, low weight and size, delayed puberty, etc.), and of course the gastroenterologist. He's 14 years old, weighs 75 lbs.
He's had a CT scan of the abdomen (normal), blood tests (including the IBD serology 7 panel) which came back not indicitive of Crohn's, a endoscopy, and two colonoscopy. We've done a stool sample check and all that they found was a bit of yeast overgrowth (no parasites or anything). They did the test for malabsorption and he's fine there.
His symptoms... abdominal pain, almost always a "3" on a scale of 1 - 10, which he just deals with, but often a 6 or 7 and sometimes a 9 or 10, where he's curled up crying. He's fatigued a lot, is very small for his age (and thin), occassionally has headaches, and has had diarrhea his entire life pretty much. Lately his pain has been so bad.
You'd think I'd just say "yay all the tests are negative, he's fine" BUT... when he was 4 years old he had illeocolic intussusception with Meckel's Diverticulum as a starting point. By the time they diagnosed that, it had turned gangrenous and they had to remove his terminal ileum, 18 inches of small intestine, and his appendix.
SO - my question - wouldn't it make it more difficult to diagnose IBD if he's missing the terminal ileum and 18" of intestine? Isn't that where it often shows up? Our GI says it would make no difference, and he may be right, but I want more opinions as that just sounds weird to me.
Ultimately I just want my son to be out of pain and "normal" but... it's a long process.
Thanks for any advice y'all have
I am trying to figure out a diagnosis for my son and I'm very frustrated. We've seen the pediatrician, the endocrinologist (for his failure to thrive, low weight and size, delayed puberty, etc.), and of course the gastroenterologist. He's 14 years old, weighs 75 lbs.
He's had a CT scan of the abdomen (normal), blood tests (including the IBD serology 7 panel) which came back not indicitive of Crohn's, a endoscopy, and two colonoscopy. We've done a stool sample check and all that they found was a bit of yeast overgrowth (no parasites or anything). They did the test for malabsorption and he's fine there.
His symptoms... abdominal pain, almost always a "3" on a scale of 1 - 10, which he just deals with, but often a 6 or 7 and sometimes a 9 or 10, where he's curled up crying. He's fatigued a lot, is very small for his age (and thin), occassionally has headaches, and has had diarrhea his entire life pretty much. Lately his pain has been so bad.
You'd think I'd just say "yay all the tests are negative, he's fine" BUT... when he was 4 years old he had illeocolic intussusception with Meckel's Diverticulum as a starting point. By the time they diagnosed that, it had turned gangrenous and they had to remove his terminal ileum, 18 inches of small intestine, and his appendix.
SO - my question - wouldn't it make it more difficult to diagnose IBD if he's missing the terminal ileum and 18" of intestine? Isn't that where it often shows up? Our GI says it would make no difference, and he may be right, but I want more opinions as that just sounds weird to me.
Ultimately I just want my son to be out of pain and "normal" but... it's a long process.
Thanks for any advice y'all have