Scleritis is a granulomatous or non-granulomatous inflammation involving the full thickness of the scleral tissue, which comprises the outer 5/6 of the fibrous tunic of the eye. Unlike the more superficial and benign episcleritis, scleritis involves the deep scleral vasculature and stroma, producing intense ocular pain that characteristically worsens with eye movement and may radiate to the periorbitalregion, temple, or jaw. The condition is characterized by deep, violaceous (bluish-red) injection of the scleral and episcleral vessels that does not blanch with topical phenylephrine — a key clinical distinguishing feature from episcleritis. Scleritis is classified anatomically as anterior (the most common, involving the anterior sclera) or posterior (involving the sclera behind the equator of the globe). Anterior scleritis is further subdivided into diffuse, nodular, necrotizing with inflammation, and necrotizing without inflammation (scleromalacia perforans). The necrotizing forms carry the most serious prognosis, with risk of globe perforation. Approximately 50% of cases are associated with a systemic condition, most commonly rheumatoid arthritis, granulomatosis with polyangiitis (formerly Wegener’s), systemic lupus erythematosus (SLE), relapsing polychondritis, inflammatory bowel disease, and reactive arthritis. Infectious etiologies (herpetic, tuberculous, syphilitic, fungal) must also be considered, particularly in cases refractory to standard therapy.
greekSclero- Greek sklēros (σκληρός) Hard, firm
-itis|Greek -itis Inflammation of
The sclera itself derives its name from its dense, tough collagen matrix. The suffix -itis denotes an inflammatory process, making scleritis literally “inflammation of the hard [coat]” — a reference to the fibrous, unyielding nature of the scleral tissue.
RELATED TERMS
episcleritis — Superficial inflammation of the episcleral tissue; milder, self-limiting, not typically associated with systemic disease; does NOT involve full scleral thickness
Uveitis — Inflammation of the uveal tract; may occur concurrently with or secondary to scleritis
Sclerocornea — Congenital opacification of the cornea, distinct from scleritis
Scleral thinning / ectasia — Sequela of necrotizing scleritis
granulomatosis with polyangiitis (GPA) — One of the most common systemic associations
Rheumatoid arthritis (RA) — Most common systemic disease linked to scleritis overall
Tenon’s capsule — Fibrous envelope surrounding the globe, often involved in posterior scleritis
Phenylephrine blanching test — Negative in scleritis (vessels don’t blanch); positive in episcleritis
CODING AND NUANCES
ICD-10-CM CODES
🔷 Scleritis — Core Codes (Category H15.0)
Code
Description
H15.001
Unspecified scleritis, right eye
H15.002
Unspecified scleritis, left eye
H15.003
Unspecified scleritis, bilateral
H15.009
Unspecified scleritis, unspecified eye
H15.011
Anterior scleritis, right eye
H15.012
Anterior scleritis, left eye
H15.013
Anterior scleritis, bilateral
H15.019
Anterior scleritis, unspecified eye
H15.021
Brawny scleritis, right eye
H15.022
Brawny scleritis, left eye
H15.023
Brawny scleritis, bilateral
H15.029
Brawny scleritis, unspecified eye
H15.031
Posterior scleritis, right eye
H15.032
Posterior scleritis, left eye
H15.033
Posterior scleritis, bilateral
H15.039
Posterior scleritis, unspecified eye
H15.041
Scleritis with corneal involvement, right eye
H15.042
Scleritis with corneal involvement, left eye
H15.043
Scleritis with corneal involvement, bilateral
H15.049
Scleritis with corneal involvement, unspecified eye
H15.091
Other scleritis, right eye
H15.092
Other scleritis, left eye
H15.093
Other scleritis, bilateral
H15.099
Other scleritis, unspecified eye
🔷 Infectious / Systemic Etiology Scleritis Codes
Code
Description
B02.34
Zoster scleritis
A18.51
Tuberculous episcleritis (note: no separate TB scleritis code; code also A18.51 + H15.0x for TB scleritis)
🔷 Related / Commonly Coded Together
Code
Description
H15.101
Unspecified episcleritis, right eye
H15.102
Unspecified episcleritis, left eye
H15.103
Unspecified episcleritis, bilateral
H15.109
Unspecified episcleritis, unspecified eye
H15.111
Episcleritis periodica fugax, right eye
H15.113
Episcleritis periodica fugax, bilateral
H15.121
Nodular episcleritis, right eye
H15.122
Nodular episcleritis, left eye
H15.123
Nodular episcleritis, bilateral
⚠️ Coder’s Note: ICD-10-CM codes in category H15 are 7 characters for most laterality-specific codes. Always assign the most specific code available. When scleritis is secondary to a systemic condition (RA, GPA, SLE, etc.), code the underlying disease first per etiology/manifestation sequencing rules if applicable. For zoster scleritis, B02.34 is a combination code and does not require an additional H15 code.
CPT CODES (Relevant to Scleritis Workup & Management)
E&M office visit codes (used when billing under medical, not ophthalmological, services)
💡 Coder’s Tip:B-scan ultrasonography (76510) is the gold standard for diagnosing posterior scleritis — the hallmark “T-sign” (fluid in Tenon’s space) is pathognomonic. Make sure documentation supports medical necessity when coding this. Also note that 92132-92134 (OCT series) are laterality-specific and should reflect documentation of which eye(s) were imaged.
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