---
title: "Cholesteatoma"
description: "ENT notes on Cholesteatoma - definition, classification, etiology, theories, clinical features, investigations, and treatment."
source: "The ENT Resident"
author: "Dr. Mausumi Das"
canonical_url: "https://www.theentresident.com/ent-notes-lectures/cholesteatoma-symptoms-treatment"
categories: ["Otology", "Mnemonics in ENT"]
video: "https://www.youtube.com/watch?v=fzVb_3KLD4c"
image: "https://media.theentresident.com/og-images/cholesteatoma-symptoms-treatment.png"
---

# Cholesteatoma

ENT notes on Cholesteatoma - definition, classification, etiology, theories, clinical features, investigations, and treatment. Watch the full video lecture on YouTube: https://www.youtube.com/watch?v=fzVb_3KLD4c

## 🧠 Cholesteatoma

### 🌬 What is Cholesteatoma?

Cholesteatoma is defined as a **benign sac of keratinizing squamous epithelium** within the **middle ear cleft** that has **bone-eroding property** and **lost its self-cleaning capacity**.

>What are the structures of the Middle Ear Cleft?

>Why is keratinizing squamous epithelium abnormal in the middle ear?

**Synonyms/Alternative Names:**
-   **Keratoma:** Signifying its keratin-filled nature.
-   **Epidermosis:** Describing its origin from squamous epithelium.

>Why is the term "Cholesteatoma" a misnomer?

---

### 🧱 Structure of a Cholesteatoma

A cholesteatoma essentially consists of two parts:

1.  **Matrix:** This is the outer sac, composed of **keratinizing squamous epithelium**. It rests on a thin layer of fibrous stroma (submucosal connective tissue). The matrix is the living, actively growing part.

2.  **Central White Mass:** This core consists of **desquamated keratin debris** (dead skin cells) that are continuously produced by the matrix. This accumulating keratin is what expands and causes pressure/erosion.

---

### 🧬 Theories of Cholesteatoma : Origin

Cholesteatoma can be classified by its origin: congenital or acquired.

Different theories explain how the keratinizing squamous epithelium enters the middle ear cleft.

📚 **Mnemonic to remember Theories of Cholesteatoma : REAL BIG EARS MAKE ECHOES**

-   **R**etraction Pocket (**Wittmaack's Theory**)
-   **B**asal cell hyperplasia (**Ruedi's Theory**)
-   **E**pithelial migration (**Habermann's Theory**)
-   **M**etaplasia (**Sade's Theory**)
-   **E**mbryonic cell rests (**Congenital Cholesteatoma**)

### 1. Congenital Cholesteatoma

-   **Definition:** An expanding cystic mass of keratinizing squamous epithelium located **medial to an intact tympanic membrane**.

-   **Theory:** Persistence of **embryonic epidermal cell rests** 

>What is Levenson's criteria for Congeintal Cholesteatoma?

-   **Common Sites:** Middle ear, Petrous Apex, Cerebellopontine Angle (CPA)

>What is the most common site for Congenital Cholesteatoma?

-   **Clinical Features:** 
    - Pearly white mass behind an intact TM
    - Conductive hearing loss. 
    
>What is the staging of Congenital Choelsteatoma?

### 2. Acquired Cholesteatoma
This type forms after birth due to various pathological processes. 

It's further divided into primary and secondary.

#### A. Primary Acquired Cholesteatoma

-   No prior history of otitis media, pre-existing perforation, or otorrhea.

-   **Theories of Origin:**

    -   Wittmaack's Theory (Invagination Theory / Retraction Pocket Theory)
    -   Ruedi's Theory (Basal Cell Hyperplasia Theory)
    -   Sade's Theory (Squamous Metaplasia Theory)

#### B. Secondary Acquired Cholesteatoma

-   Occurs in the presence of a pre-existing TM perforation (usually posterior superior marginal or large central).

-   **Theories of Origin:**

    -   Habermann's Theory (Epithelial Invasion/Migration Theory)
    -   Sade's Theory (Squamous Metaplasia Theory)

>What is Wittmack's Retraction Pocket Theory?

>What is Ruedi's Basal Cell Hyperplasia Theory?

>What is Sade's Squamous Metaplasia Theory?

>What is Habermann's Epithelial Invasion/Migration Theory?

---

### 🦴 Bone Destruction by Cholesteatoma

Cholesteatoma has a unique ability to destroy bone in its path (ossicles, bony labyrinth, facial nerve canal, sinus plate, tegmen tympani), leading to serious complications.

-   Discarded Theory: **Pressure Theory**

-   Current Theory: **Enzymatic Theory.**

>What is Pressure Theory? Why has it been discarded now?

>What is Enzymatic theory of bone destruction by Cholesteatoma?

>What is the most common bone eroded by Cholesteatoma? Why?

---

### Growth Pattern and Spread of Cholesteatoma

Cholesteatoma typically spreads in predictable patterns based on its origin site:

1.  **Posterior Epitympanum Cholesteatoma:** Spreads via:

-   Anterior Pouch of von Troeltsch → Anterior Epitympanum → Supratubal Recess/Anterior Epitympanic Sinus.

-   Posterior Pouch of von Troeltsch → Posterior Mesotympanum → Sinus Tympani/Round Window area/Facial Recess.

-   Lateral Malleal/Incudal Folds → Superior Incudal Space/Lateral Attic → Aditus ad Antrum → Antrum → Mastoid.

2.  **Posterior Mesotympanum (Inferior Incudal Space) Cholesteatoma:** Spreads via:

-   Direct spread to Sinus Tympani and Facial Recess (most common).

-   Posterior Tympanic Isthmus → Medial Attic (epitympanum medial to incus body).

-   Posterior Pouch of von Troeltsch → Prussak's space → Superior Incudal Space → Aditus → Antrum → Mastoid.

3.  **Anterior Epitympanum Cholesteatoma:** Spreads via:

-   Superiorly to Tegmen Tympani/Dura/Middle Cranial Fossa.
    
-   Anteriorly to Zygomatic Root Cells.
    
-   Can involve Geniculate Ganglion and Facial Canal.
    
-   Long-standing cases can cause Labyrinthine Fistula.

### 🦠 Microorganisms in Cholesteatoma

Polymicrobial. 
- Pseudomonas aeruginosa 
- Streptococcus
- Proteus
- E.coli
- Bacteroides
- Peptococcus
- Fusobacteria

>What is the most common organism involved in Cholesteatoma?

---

### 👶 Pediatric vs Adult Cholesteatoma

Differences in presentation and behavior:

1.  **Extent of Spread:** Pediatric cholesteatoma spreads more extensively through the temporal bone than in adults, with more involvement of perilabyrinthine cells and petrous apex.

2.  **Aggressiveness:** Pediatric cholesteatoma is generally **more aggressive** due to the more pneumatized (air-filled) temporal bone, allowing easier and more extensive spread.

3.  **Inflammatory Response:** Greater inflammatory response in children, with increased expression of markers like metalloproteinases and antibodies, leading to more bone erosion.

4.  **Labyrinthine Invasion:** Less common in pediatric cases compared to adults.

5.  **Lateral Semicircular Canal Fistula/Fallopian Canal Erosion:** Less common in pediatric cases.

6.  **Ossicular Erosion:** More common in pediatric cholesteatoma.

---

### 📋 Clinical Features of Cholesteatoma

Cholesteatoma presents as a "dangerous" form of chronic otitis media (atticoantral type).

**Symptoms:**

-   **Ear Discharge (Otorrhea):**
    -   Persistent, Foul smelling, Purulent.Often **blood stained**.

    -   Quantity: Typically **SCANTY** (as opposed to profuse in mucosal type).

    -   Continuity: Usually **Continuous** 
    
>Why is ear discharge in Cholesteatoma foul smelling and blood stained?

>Why is ear discharge in Cholesteatoma scanty and continuous?

>Why is sudden cessation of discharge in Cholesteatoma an ominous sign?

-   **Hearing Loss:** Mostly **Conductive Hearing Loss (CHL)**. Can have an SNHL component.

>What is Cholesteatoma Hearer?

-   **Bleeding from Ear:** Due to friable granulation tissue or polyps, especially on cleaning.

-   **Other Symptoms (Indicating Complications):** Patients often present with symptoms of complications due to bone erosion:
    -   Pain (persistent, deep-seated).
    -   Vertigo (labyrinthine fistula).
    -   Facial Palsy (CN VII involvement).
    -   Headache, Vomiting, Convulsions, Ataxia, Fever (intracranial spread).
    -   Tinnitus.

**Signs (On Examination):**

-   **Tympanic Membrane Perforation:**

    -   **Attic Perforation** (in pars flaccida) or **Posterior Superior Marginal Perforation** (in pars tensa, involving annulus).

-   **Retraction Pocket:** Invagination of Tympanic membrane (pars flaccida/posterior superior pars tensa). May be shallow and self-cleansing or deep with keratin accumulation.

>What is Tos Classification of Pars Flaccida Retraction?

>What is Sade Classification of Pars Tensa Retraction?

-   **Cholesteatoma:** **Pearly white flakes** (keratin debris) visible within a retraction pocket, attic, or posterior superior margin.
Congenital cholesteatoma appears as a pearl-like mass behind an intact Tympanic membrane.

-   **Osteitis / Granulation Tissue:** Fleshy red tissue coming from the attic or posterior superior margin, indicating bone inflammation.

-   **Ossicular Necrosis:** May be visible through the perforation.

-   **Cholesterol Granuloma:** Bluish mass behind TM (if intact), or yellowish/brownish if ruptured/exposed.

-   **Tuning Fork Tests:** Rinne's Negative, Weber's lateralized to the diseased ear, Absolute Bone Conduction (ABC) normal.

---

### 🔬 Investigations of Cholesteatoma

Investigations are crucial for confirming diagnosis, assessing disease extent (especially bone erosion), identifying complications, and planning surgery.

-   **Examination Under Microscope (EUM):** Priority for all cases.

-   **Pure Tone Audiometry (PTA):** When the ear is dry. 

-   **Culture & Sensitivity (C&S):** Of ear discharge (if active) to guide antibiotic therapy.

-   **Imaging:**

    -   X-ray Mastoid (e.g., Schuller's View)

    -   CT Scan of Temporal Bone (High Resolution - HRCT): **Gold standard for bony anatomy and bone erosion.**

    -   **MRI Temporal Bone:** Useful for assessing **soft tissue extension** and **intracranial complications** (e.g., brain abscess, meningitis, dural involvement). Can differentiate cholesteatoma from cholesterol granuloma or fluid. MR venography/angiography for vascular involvement.

>Why is Examination under Microscope mandatory in a case of Cholesteatoma?

>What is the purpose of doing Pure Tone Audiometry in Cholesteatoma?

>What findings do you see in CT Temporal bone in Cholesteatoma?

---

### 🏥 Treatment of Cholesteatoma

The treatment of cholesteatoma is primarily **surgical**. Medical management has a very limited role.

**Aim of Surgery:**

1.  Eradicate disease and **make the ear SAFE**.

2.  Reconstruct the hearing mechanism.

**Surgical Approaches:**

-   **Canal Wall Down (CWD) Procedures:** Remove the posterior bony EAC wall, converting the mastoid cavity and middle ear into a single, exteriorized cavity.

>What are some Canal wall down procedures you know?

>What are the advantages and disadvantages of Canal wall down procedures?

>What is Bondy's Mastoidectomy?

-   **Canal Wall Up (CWU) Procedures:** Remove disease while keeping the **posterior bony meatal wall intact**. Approach via combined access (EAC and cortical mastoidectomy).
   
>What are some Canal wall up procedures you know?

>What are the advantages and disadvantages of Canal wall up procedures?

**Reconstructive Surgery:**

-   Hearing is typically restored by **Tympanoplasty** (grafting Tympanic membrane) and **Ossicular Reconstruction** (using prostheses, sculpted ossicles, cartilage).

-   Can be performed at the **time of initial surgery** (single stage) or as a **second-stage procedure** (usually 6-12 months later) to ensure disease eradication before reconstruction.

**Conservative Management in Cholesteatoma (Limited Role):**

-   Generally **NOT** the primary treatment for cholesteatoma.

-   In these cases, polyps/granulation tissue may be surgically removed (cup forceps) or cauterized (silver nitrate).

>What are the indications for Conservative Management in Cholesteatoma?

---

## About This Note

This free ENT note on Cholesteatoma was written by Dr. Mausumi Das and is paired with a corresponding video lecture.

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