1/ This is the beginning of a #tweetorial or #pathtweetorial on a mystery topic. Fear not, it’ll become evident soon what we’re talking about. But first I’ll show you an image. These serpiginous fibroblast plugs are diagnostic if organizing pneumonia (formerly BOOP)
2/ In MOST cases of organizing pneumonia seen on lung biopsy, the etiology is not evident on histology. But sometimes, there is a clue. Examine this pic closely and then see if you can answer the quiz in the next tweet in this thread.
3/
What does the pic in the previous tweet show?
4/
Before I reveal the answer, let me show you what happened when I looked at the same field under polarized light. The particles at bottom right were birefringent but not the ones at top left. Do you know why? #pathology#pulmpath
5/
It’s because there are 2 types of pill fillers (excipients) in this image. Microcrystalline cellulose (red circle) and crospovidone (green circle). The former is colorless and brightly birefringent. The latter is purple but not birefringent. Both provide bulk to oral pills.
6/ Although pill fillers are most commonly seen in the lung in cases where people infect their pain pills intravenously (talc granulomatosis), this was not the case here. In this case, the pills were aspirated into the lung. This is “particulate matter aspiration”
7/ Several years ago, I did a study on cases like this diagnosed on lung biopsies by Dr. Katzenstein. It taught me a lot about the power of pathology as a diagnostic tool in some situations where clinical features and imaging can be VERY misleading. ncbi.nlm.nih.gov/pubmed/1746046…
8/ This is NOT the aspiration pneumonia you learn about in medical school or as a pulmonologist or ID doc.
These are not debilitated patients with GERD and a dilated esophagus, right lower lobe infiltrates and aspiration of oral flora into the lung. ❌
This is different...
9/ An important difference is that this involves aspiration of MICROSCOPIC particles (presumably from gastric contents), not bacteria from the mouth.
Also, this is not the same as finding a peanut in a bronchus. Completely different sequence of events. See next tweet...
10/ What are these aspirated particles that can show up in lung biopsies? 1. Vegetable particles 2. Meat particles (rare) 3. Pill fillers (rare) 4. Kayexalate (rare)
Meat (skeletal muscle) can be seen at autopsy but gets rapidly destroyed so is seldom seen in biopsies.
11/ When these particles enter the lung, this is the inflammatory sequence: 1. Acute bronchopneumonia and acute bronchiolitis (neutrophils) ➡️ EARLY 2. Organizing pneumonia 3. Foreign body giant cells and granulomas ➡️ late
The late changes are the most challenging...
12/ The imaging starts to get weird and deviates from standard descriptions of aspiration. You get: 1. Tree in bud opacities (reflects bronchiolitis) 2. Nodules 3. Opacities in any lobe (people aspirate when laying down) 4. Recurrent infiltrates or “recurrent pneumonia”
13/
And the pathology gets REALLY weird. It deviates from what you expect to see in aspiration pneumonia. You expect to see INTACT food particles WITHIN bronchi or bronchioles associated with acute inflammation, right? A bit like this? 👇🏾👇🏾👇🏾(that’s potato, by the way)
14/ How do I know that’s potato? When I was doing the study I embedded a bunch of different foods to see what they look like under the microscope. This was fun but of no use in real life because food degenerates when attacked by inflammatory cells for months...see next tweet
15/
In lung biopsies with particulate matter aspiration, you will see intact and degenerated vegetable particles ANYWHERE in the parenchyma, not necessarily in a lumen. There is usually a giant cell around the material, and organizing pneumonia is common.
16/ The finding of food/vegetable matter in the context of an appropriate inflammatory reaction in the lung is diagnostic of aspiration.
Food WITHIN the lung. Surrounded by inflammation!! What can be more pathognomonic of aspiration?
¯\_(ツ)_/¯
17/ Over the years, I have heard odd responses to this diagnosis:
🔴 the barium swallow is normal!
🔴 she doesn’t have GERD!
🔴 the infiltrate is not in the RLL
Yet, folks have no problem attributing any infiltrate in someone with a dilated esophagus to aspiration ¯\_(ツ)_/¯
18/ One of the most classic aspirated particles in this disease is the so-called “lentil”. It’s essentially a legume, which for some reason is aspirated a LOT and survives in the lung. First pic is a navy bean I embedded. Others are examples of lentil aspiration.
19/ Pill fillers or excipients only rarely show up in aspiration pneumonia. They are insoluble, so they can persist for long periods in the lung
Fillers in interstitium = think talc granulomatosis
Fillers associated with organizing pneumonia = consider aspiration
20/ Microcrystalline cellulose and crospovidone are often found together, presumably because they’re both used in the same pills to provide bulk and other physical properties.
Remember what they look like! This will also help you to diagnose intravenous injection of pills.
21/ And finally, you should try to learn to recognize food particles even when they’ve undergone advanced degeneration. This can be the key to making a specific diagnosis of particulate matter aspiration.
22/ Now let’s repeat the quiz I gave in the beginning of this Tweetorial to see if we made some headway and learned something. The quiz (see next tweet in thread) is based on this pic 👇🏾
For clinicians: patients with this form of aspiration often have a history of esophageal or gastric surgery (like gastric bypass) or other abnormalities, CNS diseases or drug abuse. A history of recurrent pneumonia is classic.
🔬end of Tweetorial 🔬
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Overlap is common because these abnormalities commonly occur together.
3.
Every week I will add my thoughts to this #pathtweetorial . I feel strongly about this topic because I see SO much smoking-related lung pathology that is misinterpreted and underrecognized. Not just SRIF (👇🏾) but also pigmented macrophages, commonly dismissed as “anthracotic”
1/4 (4-tweet thread)
A recent study in @ModernPathology
by Xie et el examined the ability of a deep convolutional neural network to diagnose which tumor in pleural effusions? #pathpolls
3/4
The authors claim the sensitivity and specificity of the deep convolutional neural network was somewhere between senior and junior cytopathologists. What were the numbers (sensitivity, specificity)?
cc: @DrNetto
1/ Announcing a contest to win a free pathology textbook!
Thanks to a brilliant idea by @DrMissWV and a generous offer by @science_press and @LizMontgomeryMD we are giving away a few free textbooks in an educational tweet contest called #pathbracket . See thread 👇🏾
2/
If you want to enter the contest, create a NEW educational pathology tweet between today and March 15 and tag it with #pathbracket
You must tag your own tweet. The tweet must have educational value. Tweetorials are allowed too. Contest is open to all.
3/ On March 16, #PathTweetAward judges led by @DrGeeONE will donate their time to pick 32 of the best tweets to enter in a bracket similar to #MarchMadness . Credit with the idea of a bracket goes to @DrMissWV
Progression through the bracket will be on the basis of polls.
1. How do we tell primary lung cancer from metastatic cancers from other sites?
It’s correct to say we should use all available clinical, radiologic and pathologic information, but that’s too vague to be helpful in a practical sense.
2. This #pathtweetorial is applicable mainly to #pulmpath . The principles in each organ are different. A carcinoma in a lymph node is a metastasis by definition. Not so in lung or colon.
IMHO it’s a mistake to approach a carcinoma in the lung as carcinoma of unknown primary
3. Most metastatic carcinomas to the lung occur after the primary carcinoma has already been diagnosed in another site.
💥Clinicians: give your pathologists this information! If you don’t, this is substandard, dangerous patient care.