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Concerns About Low Blood Metrics in a 14-Year-Old Girl

7/7/2025, 4:30:38 PMMale25-34

Hello everyone! I’m reaching out to share my concerns in hopes of finding some insights. My 14-year-old daughter has been experiencing some troubling lab results, including consistently low neutrophil counts (ranging from 1337 to 1459 cells/uL since December 2024, confirmed on three occasions) and a low white blood cell count of 3.4 thousand/uL, also verified three times. Recently, her ferritin levels dropped to 5 BG/ml, following a prior finding of low iron detected during a finger prick test. Additionally, in December 2024, her amylase levels were recorded at a low 13 u/l but were not retested thereafter. She was referred to a gastroenterologist due to symptoms of stomach pain, a feeling of fullness post-meals, and a burning sensation while burping. After two months of omeprazole without any improvement, the medication was halted, and the doctor suggested changes in her diet instead of pursuing follow-up care. Unfortunately, my daughter still experiences these issues. Returning to our pediatrician, we discussed starting her on iron supplements, and he advised waiting another three months for CBC results since there have been no recurrent infections. However, this approach feels unsettling to me, especially given our family medical history involving autoimmune diseases (like IBD, lupus, PsA, and RA), cancers (including pancreatic and liver), and kidney disorders (notably PKD and CKD). There's also the concern raised by a phantom lump she had in her abdomen six years ago, which disappeared before a biopsy could be performed—thanks to pandemic-related delays in healthcare services. A recent ultrasound for this site showed no abnormalities, which is a relief. My worry is that simply monitoring abnormal lab results appears more reactive than proactive. I’m unsure whether such blood discrepancies are typical for adolescents. I need to determine whether to be more assertive in seeking additional opinions, given that our pediatrician doesn't seem overly concerned—he didn't even reach out to discuss the abnormal lab results apart from the ferritin levels, and I had to chase answers regarding the amylase levels in December. Should I accept this typical lapse in concern or consider finding a new physician willing to advocate for further tests or potential referrals to specialists? I appreciate any guidance you can provide!

AgingSupplementsFamily Medicine

Answers (1)

Cony

7/7/2025, 4:31:05 PM

OpenHealth AI

Your concerns about your daughter's lab results and ongoing symptoms are valid and important to address. It’s understandable to feel unsettled when faced with such health issues, especially with a family history of serious conditions. Here's a structured way to approach your situation:

Main Points:

  1. Low blood metrics indicate potential health concerns that warrant close attention.
  2. Persistent symptoms and low iron levels suggest further investigation may be necessary.
  3. Advocating for your daughter's health is crucial, especially given your family's medical history.

Explanation:

Low neutrophil counts (which play a role in fighting infections), low white blood cell counts, and low ferritin levels can all signal underlying health issues, such as nutritional deficiencies, bone marrow problems, or chronic conditions. Your daughter’s gastrointestinal symptoms, such as stomach pain and fullness after meals, add more complexity to her situation. While some fluctuations in lab values can occur during adolescence, persistent abnormalities should not be overlooked.

Next Steps:

  1. Document Symptoms and Changes: Keep a detailed diary of her symptoms, dietary habits, and any changes in her physical state. This information will be valuable for any healthcare provider you consult next.

  2. Obtain a Second Opinion: Consider seeking a second opinion from a pediatric hematologist or a gastroenterologist, particularly one specializing in adolescents. This will allow you to explore all potential causes and management options.

  3. Ask for Comprehensive Testing: Request your healthcare provider to perform additional tests to assess her iron levels further (including complete iron studies) and any other relevant tests for gastrointestinal issues. This can include testing for autoimmune markers given your family history.

  4. Explore Dietary Adjustments: While not a substitute for medical evaluation, ensuring that your daughter is getting iron-rich foods (like leafy greens, beans, and lean meats) and foods rich in vitamin C (to enhance iron absorption) may help alongside any supplements prescribed.

  5. Regular Follow-Up: Stay proactive in scheduling follow-up appointments to review her lab results and symptoms. If her pediatrician does not respond adequately to your concerns, consider looking for a new physician who prioritizes thorough investigations and advocates for your daughter’s health.

Your daughter deserves attentive care and monitoring, especially in light of her symptoms and historical health concerns. Trust your instincts as a parent; advocating for her health is not only appropriate but necessary.

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