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Case report review of clindamycin use in a 62-year-old male with Neurofibromatosis type 1 and hematomaA Rare Bleeding Complication Every NF1 Patient Should Know About

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Key Takeaway
Note that acute pain or unexplained mass in NF1 suggests spontaneous hemorrhage requiring prompt imaging.

This source is a case report review focusing on a single 62-year-old male patient with Neurofibromatosis type 1. The clinical scenario involved the management of a hematoma through a combination of transcatheter arterial embolization, ultrasound-guided drainage, debridement, and targeted antibiotic therapy using clindamycin. No comparator group was reported for this individual case. The primary outcome of hematoma volume drained was approximately 3000 mL of old blood. Secondary outcomes included hematoma rupture and secondary infection, which were observed as adverse events in this specific instance. Follow-up duration was not reported. The review does not provide pooled effect sizes or data from a larger sample size. The authors emphasize that acute pain or an unexplained mass in an NF1 patient should raise immediate suspicion for spontaneous hemorrhage. This clinical presentation necessitates prompt vascular imaging and multidisciplinary intervention to improve outcomes. The certainty of these findings is limited by the small sample size inherent to a case report. Practice relevance is framed around the need for vigilance in NF1 patients presenting with these specific symptoms.

What is NF1 and why does this matter

NF1 is a genetic disorder that affects about 1 in 3,000 people worldwide. It causes tumors to grow on nerves. But it also affects blood vessels.

Most people with NF1 know about the skin changes and the risk of nerve tumors. What many don't know is that their blood vessels can be fragile too. The walls of arteries can become weak and thin. This is called vascular dysplasia.

When an artery ruptures on its own, it can cause a hematoma. That is a large collection of blood outside the blood vessel. In this case, the hematoma was in the lower back and buttock area. It held about 3 liters of blood.

The old way versus what we now know

Doctors have known for years that NF1 can affect blood vessels. But spontaneous rupture was considered extremely rare. Most cases were found only after death.

Here's the twist. This case shows the full picture from start to finish. The patient survived. Doctors were able to track exactly what happened and how they treated it.

The old thinking was that sudden pain and swelling in NF1 patients was probably a tumor or an infection. The new thinking is that doctors should also consider a bleeding artery. This changes how quickly they act.

How a blood vessel fails in NF1

Think of a healthy artery like a strong garden hose. The walls are thick and flexible. They can handle normal pressure.

In NF1, the artery walls can become thin and weak. It is like that same hose developing a thin spot. Over time, that spot bulges. Eventually, it can burst.

The NF1 gene affects a protein called neurofibromin. This protein helps control cell growth. Without enough of it, cells in the blood vessel walls grow abnormally. The walls become disorganized and fragile.

This is not something you can feel or see from the outside. It happens silently inside the body.

The patient was a 62-year-old man with known NF1. He came to the hospital with sudden pain on his left side. There was swelling in his lower back and buttock area.

Doctors did a CT scan. They found a large hematoma. They also found a mass near the tailbone.

Next, they did an angiogram. This is a special X-ray that shows blood vessels. They found active bleeding from two arteries. One was the left second lumbar artery. The other was the subcostal artery.

Doctors stopped the bleeding using a procedure called transcatheter arterial embolization (TAE). They inserted a thin tube into the artery and blocked it off.

The results that matter for patients

The bleeding stopped. That was the good news.

But the story did not end there. About 3 liters of old blood had collected in the tissues. This caused pressure and damage. The hematoma later ruptured through the skin. It also became infected.

Doctors had to drain the blood using ultrasound guidance. They cleaned out the damaged tissue. They gave antibiotics to fight the infection.

The patient recovered. But it took multiple procedures and weeks of care.

This does not mean every NF1 patient will have this complication. It is rare. But knowing the warning signs could save a life.

What experts say about this case

The authors of the report emphasize one key point. Any NF1 patient with sudden pain or an unexplained lump should be checked for bleeding right away.

They call this the "complete clinical trajectory" of spontaneous artery rupture in NF1. It starts with a bleed. Then a hematoma forms. Then complications like infection can follow.

The message is clear. Do not assume it is just a tumor or a muscle strain. Get imaging done quickly.

What this means for you or your loved one

If you have NF1, you do not need to live in fear. But you should know the signs.

Sudden pain in the back, abdomen, or side. Swelling that appears quickly. A lump that was not there before. These are reasons to seek medical help immediately.

Tell the doctor you have NF1. Mention that blood vessel problems can happen. Ask for a CT scan or ultrasound if there is any concern.

This treatment is available now. Embolization is done in many hospitals. Drainage and antibiotics are standard care. The key is catching it early.

The honest limitations

This is a single case report. That means it describes one person. It does not prove how often this happens or who is most at risk.

The patient was older. Most NF1 patients are diagnosed in childhood. We do not know if younger patients face the same risk.

Also, the patient had no known blood vessel problems before this event. There is no way yet to predict who might have fragile arteries.

What happens next

Researchers need to study more cases. They need to understand why some NF1 patients develop weak artery walls and others do not.

For now, the main takeaway is awareness. Doctors who treat NF1 patients should think about blood vessel problems. Patients and families should know the warning signs.

Research takes time. But this case gives doctors a clear picture of what to look for. And that could save lives.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Neurofibromatosis type 1 (NF1) is a multisystem genetic disorder in which vascular dysplasia can lead to rare, life-threatening spontaneous hemorrhage. We present the case of a 62-year-old male NF1 patient who presented with acute left lumbar pain and swelling without a history of trauma or anticoagulant use. Computed tomography (CT) revealed a large hematoma in the left lumbogluteal region and a presacral mass. Active bleeding from the left second lumbar artery and the subcostal artery was confirmed by digital subtraction angiography and successfully managed with transcatheter arterial embolization (TAE). The postoperative course was complicated by hematoma rupture and secondary infection. This was controlled with ultrasound-guided drainage (yielding approximately 3000 mL of old blood), debridement, and targeted antibiotic therapy (clindamycin). This case illustrates the rare yet complete clinical trajectory of spontaneous arterial rupture in NF1, from massive hematoma formation to infectious complications. It underscores that acute pain or an unexplained mass in an NF1 patient should raise immediate suspicion for spontaneous hemorrhage, necessitating prompt vascular imaging and multidisciplinary intervention to improve outcomes.
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