Tumor
Hello Doctor: My daughter is 4 years old, and she has developed a tumor at the coccyx (sacral area).
She underwent surgery last May, and the pathology report indicated two possibilities: 1.
Juvenile Xanthogranuloma 2.
Aneurysmal Bone Cyst.
It is uncertain which type of tumor it is, and now it has recurred and grown (approximately 6 cm wide and 4 cm deep).
It is evident that surgery could not completely remove it, as it is adhered to the nerves.
I would like to ask: what are these two types of tumors? Besides surgery, are there any other treatment options available?
Youying de mama, 30~39 year old female. Ask Date: 2005/04/27
Dr. Li Wenlin reply Orthopedics
Hello,
In response to your inquiry, your daughter's condition is not a common case.
I personally recommend taking her to see Dr.
Chen Tian-Hsiung or Dr.
Chen Wei-Ming at Taipei Veterans General Hospital's Orthopedic Department, or Dr.
Yang Rong-Sen at National Taiwan University Hospital.
It would be best to prepare a summary of her medical history, surgical records, and pathology reports.
These specialists are authorities in this field, and consulting them will ensure that your daughter receives the best possible treatment.
Online consultations can be challenging in terms of depth and specificity; merely discussing literature cases may seem impersonal, while superficial responses may not satisfy your concern for your beloved daughter.
Please seek a referral for treatment as soon as possible.
Wishing her a speedy recovery.
Reply Date: 2005/04/27
More Info
Juvenile Granuloma and Aneurysmal Bone Cysts (ABCs) are two distinct types of tumors that can occur in children, and understanding their characteristics, treatment options, and implications is crucial for managing your daughter's condition.
Juvenile Granuloma (also known as Pyogenic Granuloma) is a benign vascular tumor that often appears as a raised, red lesion on the skin or mucous membranes. It is most commonly found in children and can occur following trauma or irritation. While it is not cancerous, it can be locally aggressive and may recur after removal. The treatment typically involves surgical excision, but complete removal can be challenging, especially if the lesion is large or adheres to surrounding tissues, such as nerves.
Aneurysmal Bone Cyst (ABC), on the other hand, is a benign but locally aggressive bone lesion characterized by blood-filled cystic spaces. ABCs can occur in any bone but are most commonly found in the long bones and the spine. They often present in children and adolescents and can cause pain, swelling, and sometimes fractures. The treatment for ABCs usually involves curettage (surgical scraping) of the cyst and may be followed by bone grafting to fill the defect. In some cases, additional treatments such as sclerotherapy (injecting a substance to close off the cyst) or embolization (blocking the blood supply to the cyst) may be considered to reduce the risk of recurrence.
In your daughter's case, the fact that the tumor has recurred and grown significantly indicates that it may be challenging to manage solely through surgery, especially if it is adhering to nerves. Here are some considerations regarding treatment options:
1. Surgical Options: If the tumor is accessible and the surgical team believes they can achieve a clean margin, another surgical intervention may be warranted. However, if the tumor is deeply embedded or adherent to critical structures, the risks of surgery may outweigh the benefits.
2. Non-Surgical Treatments: Depending on the specific diagnosis, non-surgical options may be available. For example, if the tumor is diagnosed as an ABC, sclerotherapy or embolization could be considered to reduce the size of the cyst and minimize the risk of further complications.
3. Observation: In some cases, if the tumor is not causing significant symptoms or complications, a watchful waiting approach may be appropriate, especially if the tumor is benign and not rapidly growing.
4. Multidisciplinary Approach: It may be beneficial to consult with a pediatric oncologist, orthopedic surgeon, and possibly a neurosurgeon, given the tumor's proximity to the nerves. A multidisciplinary team can provide a comprehensive treatment plan tailored to your daughter's specific situation.
5. Follow-Up Care: Regular follow-up with imaging studies (such as MRI or CT scans) will be essential to monitor the tumor's behavior over time, especially if you opt for a non-surgical approach.
In conclusion, both Juvenile Granuloma and Aneurysmal Bone Cysts are benign tumors, but they require careful evaluation and management due to their potential for recurrence and complications. It is crucial to have a detailed discussion with your healthcare team about the best course of action for your daughter, considering her specific diagnosis, the tumor's behavior, and her overall health.
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