OpenHealth Q&A

Get answered by medical professionals

Surgeon's Advice on Gallbladder and Hernia Surgery

9/13/2025, 8:01:32 AMMale25-34

**Patient Profile** - **Age:** 28 - **Gender:** Male - **Height:** 178 cm - **Weight:** 68 kg **Medical History:** Eight years ago, I underwent surgery for an intestinal perforation, and since then, I have developed a hernia directly below the incision site. I do not smoke and consume alcohol sparingly, typically on special occasions like birthdays or festivals. In a recent ultrasound, doctors identified four gallbladder polyps that do not cast shadows, with the largest measuring approximately 3.5 mm. My physician has informed me that even these small polyps carry a risk of becoming cancerous and could also cause digestive issues, regardless of malignancy. I am prepared to proceed with the hernia surgery, but I have significant apprehension regarding the potential removal of my gallbladder. Should I consider gallbladder excision in conjunction with the hernia operation, or should my focus remain solely on addressing the hernia? I welcome any insights or personal experiences you may wish to share. Thank you!

Multiple SclerosisCrohn's DiseaseInternal Medicine

Answers (1)

Cony

9/13/2025, 8:02:09 AM

OpenHealth AI

It’s understandable to feel apprehensive about surgery, especially when considering multiple procedures like hernia repair and potential gallbladder removal. Here’s a breakdown of the situation and guidance on how to move forward.

Understanding Your Situation:

  1. Hernia Repair: Addressing the hernia is important, especially considering it developed at a previous surgical site. Repairing it will relieve discomfort and prevent complications.

  2. Gallbladder Polyps: Small gallbladder polyps, particularly under 1 cm, are often monitored since they have a low risk of being cancerous. However, factors like your medical history and symptoms (if any) can influence the decision on whether to remove the gallbladder.

Next Steps to Consider:

  1. Consult with Your Surgeon: Since you're already prepared for hernia surgery, discuss your concerns about gallbladder removal with your surgeon. They can provide specific insights based on your ultrasound findings and overall health.

  2. Weighing Options:

    • If your gallbladder is not causing significant symptoms and the polyps are small, your surgeon may recommend monitoring them rather than immediate removal.
    • However, if you have frequent symptoms like pain or digestive issues that could be attributed to gallbladder problems, they might suggest removal during the hernia surgery for a more comprehensive treatment.
  3. Consider Comprehensive Care: If you decide to have both surgeries, it may minimize recovery time since you'll undergo anesthesia and recovery only once. Discuss with your healthcare provider the potential benefits versus risks of combining the procedures.

Self-Care and Preparation:

  • Prepare for Surgery: Engage in pre-surgical preparations, including a healthy diet, staying hydrated, and following any specific guidelines your doctor provides.
  • Monitor Symptoms: Pay attention to any changes in symptoms related to both the hernia and potential gallbladder issues leading up to your surgery.

Conclusion:

Ultimately, the best way forward involves communicating openly with your surgical team about your concerns and the potential risks and benefits of both procedures. They can help you make a well-informed decision that aligns with your health needs and comfort level. If you have more questions or need additional support, feel free to ask!

Related Questions

Dark Flickering at the Periphery of Vision

Today, I (18 male) awakened to find that I had a fever of 102 degrees. After spending most of the day resting, I began to notice a peculiar issue: when I turned my gaze to the left, I saw a dark, flickering sensation at the outer edge of my left eye's field of vision. It's difficult to articulate exactly what it looks like. I have nearsightedness with a vision correction of -5.5. Should I be worried about this? The flickering is subtle and only becomes apparent when I focus on it.

Thyroid DisordersInternal MedicineEndocrinology
Male25-34
37 minutes ago

Identifying Seriousness in Prolonged Abdominal Discomfort

Age: 24, Gender: Female, Height: 5'2", Weight: 121 lbs. Diagnosed with PCOS, but no significant medical history and no surgical interventions to date. Chronology of Symptoms: - **Sept 4-6**: I experienced the beginning of sharp pain in the upper right section of my abdomen. The discomfort felt like stabbing or creeping sensations, typically lasting only a few seconds but consistently located in the same area. - **Sept 7**: The pain became less localized, leading to more generalized discomfort in the upper abdomen. - **Sept 8**: I noticed a peculiar pulsing feeling akin to a heartbeat in my abdominal area. Additionally, my bowel habits changed, with softer stools occurring more frequently than normal. My stomach began making loud gurgling sounds. - **Sept 9-13**: Ongoing discomfort persisted in the upper abdomen. A new development was an urgent urge to relieve myself shortly after I eat, which became a daily occurrence. My stools remained soft. I have scheduled an abdominal and pelvic ultrasound for Monday and have been directed to a gastroenterologist. However, I haven't received any guidance regarding what these symptoms might indicate or what steps I should take while awaiting these scans, with the specialist's visit potentially several weeks away. I'm looking for insights on what these symptoms might suggest.

Crohn's DiseaseThyroid DisordersInternal Medicine
Male25-34
2 hours ago

Distinguishing Between Typical Discomfort and Alarming Pain After Tibial Stress Reaction

At 20 years old, I received a diagnosis of a tibial stress reaction which led to a six-week hiatus from running, occurring 11 weeks ago. Although I rested for the initial six weeks, I continued to experience discomfort in my leg, prompting me to extend my break from physical activity. Recently, my orthopedic specialist has given me the go-ahead to gradually resume running, on the condition that I am free from pain. Walking no longer causes any pain, so I attempted to jog. While jogging, I didn't experience pain, though I could feel pressure and a sense of my bone. However, shortly after my jog and the following day, I did feel some pain when walking. I've been diligently taking Vitamin D and calcium supplements, ensuring I rest adequately. Given my youth, I wonder if my concerns are unfounded. I doubt that I've sustained another injury, yet I realize I need to navigate through discomfort to return to my routine. Unfortunately, I struggle to discern between pain that is simply a part of recovery and pain that signals something more serious. - I experience irregular menstrual cycles, likely due to excessive training. - The stress reaction arose from my intense workout regimen. - As an athlete, I push my limits often.

ArthritisCOPDInternal Medicine
Male25-34
2 hours ago

What Steps to Take After Possible Bat Bites?

Demographics: Male, 17 years old, from Iași, Romania, height of 170 cm. Current medications: None. About two days ago, I discovered two unusual marks on my leg, spaced less than a centimeter apart, shortly after spotting a bat near my apartment. My relationship with my parents has been challenging; they have largely neglected me throughout my upbringing. Lately, their disregard for my health has reached alarming levels—they leave my medical issues unresolved and push me to engage in sports, even when my doctor has advised against it. I am quite certain that I won’t receive the rabies vaccination through them. If I seek help on my own, there’s a risk that child protective services might get involved. This situation could lead to severe consequences, including potential physical punishment from my parents or being put into isolation, which would prevent me from establishing my independence when I turn 18. This would leave me without an ID and without a place to live, as they would obstruct me from changing my address to theirs. More details are available in the comments.

ArthritisLupusInternal Medicine
Male25-34
2 hours ago

Understanding Migraine-Related Nerve Sensations

Hello everyone, I’m a 34-year-old male, weighing approximately 90 kg, and I generally maintain a good level of fitness. Despite my involvement with multiple specialists, I’m not seeking a formal diagnosis at this stage. I previously shared my experiences in a neurology group and hope to gain additional insights from a broader audience of doctors. While I am not trained in medicine or neurology, my background as a geotechnical engineer has led me to develop unusual nerve sensations in my head and face. I reside in Sydney, Australia, where I have consulted with reputable neurologists. I’d like to share what has been troubling me since my last visits to both a neurologist and a neurosurgeon. I apologize for the lengthy explanation but aim to make it clearer. About two years ago, while traveling, I began experiencing excruciating headaches on almost a daily basis—what I would describe as migraines or something similar in intensity. Following my return from that trip (which lasted a month), I noticed a tightness in my forehead, akin to a rubber band, which later transitioned into a sharp pain in the back of my head that varied in intensity and duration. After several consultations with general practitioners, physiotherapists, and even a chiropractor (a decision I regret), I finally consulted a neurologist who diagnosed me with secondary occipital neuralgia, likely triggered by muscle spasms, and began Botox treatments. However, the results were not satisfactory. A month later, I began to feel stabbing pain around my nasal area, which sometimes spread to my eye or cheek. This pain often coincided with my occipital discomfort, or occurred on its own. The same neurologist attributed this new symptom to Sluder's neuralgia (sphenopalatine) and prescribed Gabapentin, which provided no relief whatsoever and significantly impacted my quality of life. After two to three months of persistent pain and mental distress, I consulted with a retired neurosurgeon client of mine, who, due to ethical retirement restrictions, couldn't provide direct advice but encouraged me to seek a second opinion. The second neurologist contradicted my prior diagnoses, stating he had never encountered a genuine case of sphenopalatine neuralgia in his 40 years of practice. He told me that having both neuralgias was very unlikely and suggested that I was experiencing anxiety instead. He prescribed Effexor at a 75 mg dosage, which did help mitigate my symptoms, though not eliminate them. After six months, I found myself visiting a cousin in France, who introduced me to a well-respected neurosurgeon known for his expertise in France, Lebanon, and the UAE. This specialist also suspected that my condition was not true neuralgia but suggested it might be a form of craniofacial pain. He recommended continuing with Effexor for another six months, avoiding any research on neuralgia online, and suggested trying CQ10 as a supplement. Six months later, while the sensations persisted, they were less intense than at their onset. I approached another neurologist in Sydney, who is an expert in headache and migraine disorders. After a thorough evaluation, he concluded that I did not suffer from true neuralgia, which typically causes severe and immobilizing pain. Instead, he indicated I was experiencing a variant of migraines associated with craniofacial pain linked to the occipital and trigeminal nerves. He advised discontinuing Effexor as planned and starting treatment with Adjovy. I recently completed my fourth monthly dose of Adjovy, and I am noticing a reduction in the intensity and duration of these nerve sensations. Now, they occasionally manifest as an ongoing flickering light around the base of my nose, sometimes extending towards my eye area. The occipital region may feel itchy, slightly burning, or even stinging in certain spots, but these sensations rarely radiate. It's important to note that I haven't experienced severe headaches since these issues began. The sensations aren't sharp electric shocks as described in typical neuralgias; rather, they linger for varying durations, from minutes to hours. I am curious about how migraines could lead to these nerve sensations that I've described. My neurologist and the neurosurgeon simplified it by explaining that, instead of classic migraine-related pain, my experiences are expressed through the nerves that are typically responsible for such headaches. I appreciate your patience in reading this message. I’m hopeful for some understanding and clarification regarding how these nerve sensations relate to migraines, preferably in straightforward, accessible terms. That way, I can reinforce the notion that these sensations are merely migraine-related and try to lessen my focus on them.

Multiple SclerosisCrohn's DiseaseThyroid Disorders
Male25-34
2 hours ago