This Clinical Documentation Guide (CDG) covers non-pressure, non-venous chronic skin ulcers — primarily the FY2026 ICD-10-CM categories L97 (non-pressure chronic ulcer of lower limb, not elsewhere classified) and L98.4 (non-pressure chronic ulcer of skin, not elsewhere classified). Pressure ulcers (L89) and venous stasis ulcers (I87.2, I83.0–I83.2) are distinct conditions with their own CDGs — this guide links to both where appropriate. Content is intended for AAPC/AHIMA-credentialed coders, CDI specialists, and auditors working in wound care, vascular surgery, podiatry, and complex medical-surgical settings.
Pressure ulcers (L89.x): Stage I–IV and unstageable pressure injuries have their own CDG. Link: Pressure Ulcers CDG (see CCO Clinical Documentation Guides index).
Venous stasis ulcers (I87.2xx, I83.0xx–I83.2xx): Chronic venous insufficiency with ulceration is governed by different etiology, HCC mapping, and coding rules. Link: Venous Ulcers / Chronic Venous Insufficiency CDG.
1. Definition
A non-pressure, non-venous chronic skin ulcer is a full-thickness skin defect of at least 4–6 weeks' duration that does not result primarily from sustained pressure over a bony prominence and is not caused primarily by venous hypertension or venous insufficiency. These ulcers arise instead from arterial insufficiency, neuropathy (especially diabetic), vasculitis, inflammatory dermatoses (pyoderma gangrenosum, calciphylaxis), trauma, malignancy, or a combination of etiologies, as classified by the CDC/NCHS ICD-10-CM classification.
The ICD-10-CM categories L97 and L98.4 are residual "not elsewhere classified" (NEC) categories, meaning they apply only when the ulcer cannot be more specifically assigned to a condition-specific code (e.g., diabetic foot ulcer combination code E11.621 + L97.5xx, or arterial ulcer from atherosclerosis I70.2xx–I70.7xx). Documentation of etiology is therefore critical to accurate code assignment, as detailed in the FY2026 ICD-10-CM Official Coding Guidelines.
Depth (severity) is the single most important documentation element for these codes — the 6th character determines whether HCC v28 RAF credit is generated, and the difference between a shallow ulcer (skin breakdown only) and one exposing fat, muscle, or bone can change risk-adjusted reimbursement by hundreds of dollars per member per year.
2. Alternative Terminology
| Formal / Clinical Term | Colloquial / Lay / Alternate Name |
|---|---|
| Non-pressure chronic ulcer of lower limb (L97) | Leg ulcer, lower extremity ulcer, foot ulcer (when not diabetic or venous) |
| Arterial ulcer / ischemic ulcer | Poor circulation wound, peripheral arterial disease (PAD) ulcer, dry gangrene wound |
| Diabetic foot ulcer (DFU) | Diabetes-related foot wound, neuropathic ulcer, Charcot foot wound |
| Neuropathic ulcer (non-diabetic) | Pressure neuropathy wound, sensory loss ulcer |
| Pyoderma gangrenosum | PG ulcer, inflammatory ulcer |
| Calciphylaxis ulcer | Calcific uremic arteriolopathy wound, CUA |
| Vasculitic ulcer | Autoimmune ulcer, lupus ulcer, rheumatoid vasculitis wound |
| Non-pressure chronic ulcer of skin NEC (L98.4) | Trunk ulcer, back wound, buttock wound (non-pressure), abdominal wall ulcer |
| Necrosis of skin/subcutaneous tissue | Dead tissue wound, black eschar, necrotic wound |
| Ulcer with muscle or bone involvement | Deep wound, infected bone wound, osteomyelitis wound |
3. Signs & Symptoms
Clinical presentation varies significantly by etiology but shared features include:
- Location: Lower extremity (thigh, calf, ankle, heel, dorsum of foot) for L97; trunk, back, buttock, and non-lower-extremity sites for L98.4
- Ulcer bed: May be pale/sloughy (arterial/ischemic), pink/granulating (healing), yellow/necrotic (infected or avascular), or black/eschar (dry necrosis)
- Wound edges: Punched-out (arterial), irregular/undermined (neuropathic), violaceous/irregular (pyoderma gangrenosum), or stellate (vasculitic)
- Pain: Often severe and worsening at night in arterial ulcers; notably absent in neuropathic ulcers; moderate in venous (distinguish from L97/L98.4 scope)
- Surrounding skin: Pallor, dependent rubor, hair loss, and shiny atrophic skin (arterial); hyperpigmentation (post-inflammatory); normal to indurated (neuropathic)
- Palpable pulses: Diminished or absent dorsalis pedis / posterior tibial pulses (arterial)
- Associated symptoms: Claudication, rest pain, sensory neuropathy, autonomic neuropathy signs (anhidrosis, warm foot in Charcot)
- Signs of infection: Erythema, warmth, purulent discharge, malodor, crepitus (gas-forming organisms), fever, leukocytosis
- Depth indicators documented by clinicians: "Skin breakdown only," "fat visible," "tendon/muscle exposed," "bone visible" or "probing to bone positive" — each maps to a different 6th-character depth code
When the progress note documents a foot/leg ulcer in a diabetic patient with peripheral neuropathy and notes the patient feels no pain, this is a clinically significant neuropathic finding — not reassuring documentation. Query the provider to confirm neuropathic etiology, which affects both the combination code selection (E11.621) and the absence/presence of peripheral neuropathy (E11.40/E11.49).
4. Differential Diagnosis
| Condition | Key Distinguishing Features | Primary ICD-10-CM |
|---|---|---|
| Arterial / ischemic ulcer | Punched-out, pale/necrotic base; absent/diminished pulses; ABI <0.9; rest pain; distal foot/toe location; associated with I70.2xx–I70.7xx atherosclerosis | I70.231–I70.799 (atherosclerosis of native/bypass arteries with ulceration/gangrene); also L97.x for anatomic ulcer site |
| Diabetic foot ulcer | Plantar or pressure-point foot; neuropathy predominant; warm foot; absent pain; associated hyperglycemia; positive 10g monofilament loss | E11.621 (Type 2 DM with foot ulcer) + L97.5xx; E10.621 (Type 1) |
| Pressure (decubitus) ulcer | Over bony prominence; bed/wheelchair-bound; staged I–IV; sacrum, heel, occiput most common | L89.xxx — SEPARATE CDG |
| Venous stasis ulcer | Medial malleolus; shallow, irregular; hemosiderin/lipodermatosclerosis; painless to moderate; varicosities visible/palpable | I87.2xx, I83.0xx–I83.2xx — SEPARATE CDG |
| Pyoderma gangrenosum (PG) | Violaceous border; pathergy; painful; associated IBD, RA, hematologic malignancy; L98.4xx or L88 (specific code) | L88 (pyoderma gangrenosum) with L98.4xx for anatomic ulcer description if needed |
| Calciphylaxis (CUA) | Renal failure / dialysis patient; stellate necrotic plaques; proximal lower extremity or trunk; extremely painful; calcium deposits on biopsy | E83.59 + L98.49x or L97.xx depending on site |
| Vasculitic ulcer | Associated autoimmune disease (SLE, RA, ANCA vasculitis); palpable purpura; abnormal ANCA/ANA/complement; punch biopsy showing vessel inflammation | M05.xx, M32.xx, M31.xx + L97.xx or L98.4xx |
| Malignant ulcer (Marjolin's) | Longstanding wound; elevated or rolled edges; friable tissue; failure to heal; biopsy confirming SCC/BCC | C44.xxx (malignant neoplasm of skin) |
| Traumatic ulcer / surgical wound dehiscence | Clear precipitating event; acute rather than chronic; post-operative site | T79.3xxA, T81.3xxA, T81.4xxA |
| Neuropathic ulcer (non-diabetic) | B12/folate deficiency neuropathy, leprosy, spinal cord injury — weight-bearing surface; sensory loss | L97.xxx + underlying neuropathy code |
5. Clinical Indicators for Coders / CDI
| Clinical Indicator | CDI / Coding Significance | Action Required |
|---|---|---|
| Wound depth documented (skin, fat, muscle, bone) | Drives 6th character; determines HCC assignment; critical for RAF | Verify 6th char matches documented depth every encounter |
| Laterality documented (right, left) | Required 5th character; unspecified laterality downcodes | Query if laterality absent in chronic wound note |
| Etiology documented (arterial, diabetic, vasculitis) | Determines whether L97/L98.4 or more specific code applies | Query provider for etiology when not documented |
| Diabetes with foot ulcer combination | E11.621 + L97.5xx always coded together; never L97.5xx alone in DM patient without E-code | Verify E11.621 present whenever L97.5xx used in diabetic patient |
| Atherosclerosis with ulceration | I70.2xx–I70.7xx with ulceration subsumes arterial ulcer; L97 added for anatomic detail | Confirm I70.xxx is PDx when PAD is primary etiology |
| Bone involvement / probing to bone | Suggests osteomyelitis (M86.xx); triggers L97.xx4 or L97.xx6 6th char | Query for osteomyelitis confirmation if "bone probe positive" |
| Infection documented | L08.9 (local infection, unspecified) or specific organism codes (B95.x, B96.x); may add MS-DRG weight | Identify causative organism; add wound culture results as additional diagnoses |
| Gangrene present | I96 (gangrene NEC) should be coded additionally; HCC 263 relevant | Confirm gangrene documentation; code I96 as additional if clinician confirms |
| Multiple ulcers (bilateral or multiple sites) | Each anatomically distinct ulcer with different depth requires separate code | Code each ulcer separately per FY2026 Guidelines Section I.C.12.a.6 |
| Wound size/dimensions | Not captured in ICD-10-CM code but supports medical necessity for wound care CPT billing | Document cm² for skin substitute/graft billing |
The single most common CDI miss in wound care coding is failure to document wound depth in clinical notes. Coders default to 6th character "0" (unspecified) or "1" (skin breakdown only) when the actual wound may expose fat (code 2), muscle (codes 3 or 5), or bone (codes 4 or 6). This error systematically forfeits HCC v28 credit (HCC 380, RAF ~0.670) and may trigger RAC/MAC audit recoveries for underdocumented high-complexity claims. Depth documentation must appear in every wound care encounter note, not just the initial assessment.
6. Anatomy & Pathophysiology
Relevant Anatomy
The skin is a layered organ comprising the epidermis (outermost; keratinized stratified squamous epithelium), the dermis (collagen/elastin matrix, hair follicles, sweat glands, sensory nerves, blood vessels), and the hypodermis/subcutaneous fat layer (adipose connective tissue serving as insulation and vascular conduit). Below the skin lie fascia, muscle, tendon, and bone. The 6th-character depth codes in L97 and L98.4 directly map to these anatomic layers, as described in the NCBI anatomy reference (StatPearls — Integumentary System):
- 6th char 1 — Skin breakdown only: Ulcer limited to epidermis ± superficial dermis
- 6th char 2 — Fat layer exposed: Full-thickness dermis destroyed; subcutaneous fat visible
- 6th char 3 — Necrosis of muscle: Full-thickness wound with muscle necrosis (myonecrosis)
- 6th char 4 — Necrosis of bone: Bone exposed and/or necrotic (osteonecrosis); consider M86 osteomyelitis
- 6th char 5 — Muscle involvement without necrosis: Muscle exposed but viable; tendon visible
- 6th char 6 — Bone involvement without necrosis: Bone visible/probed but not necrotic; high infection risk
- 6th char 8 — Other specified severity
- 6th char 9 — Severity unspecified (documentation inadequate)
Pathophysiology by Etiology
Arterial/Ischemic: Peripheral arterial occlusive disease (PAOD) reduces tissue oxygen delivery. ABI <0.4 indicates critical limb ischemia. Tissue hypoxia causes coagulative necrosis; wounds fail to granulate. Per AHA/ACC 2024 Peripheral Artery Disease Guidelines, critical limb-threatening ischemia (CLTI) is defined by rest pain, gangrene, or ischemic wounds.
Diabetic Neuropathic: Sensory neuropathy eliminates protective pain sensation; motor neuropathy causes foot deformity (claw toes, Charcot); autonomic neuropathy produces dry skin and fissures. Repetitive mechanical trauma on insensate skin creates plantar ulcers at pressure points. Hyperglycemia impairs neutrophil chemotaxis, collagen synthesis, and angiogenesis. The ADA Standards of Care 2024 classify diabetic foot ulcers using the Wagner or PEDIS systems and emphasize the combination E11.621 + L97.5xx as the mandatory coding pair.
Inflammatory/Vasculitic: Immune-complex deposition or neutrophilic infiltration (pyoderma gangrenosum — L88) causes tissue destruction. Calciphylaxis involves medial calcification and thrombosis of dermal arterioles in CKD stage 4–5/dialysis patients, producing ischemic necrosis. Per StatPearls — Calciphylaxis, mortality is 45–80% at 1 year.
Wound Healing Biology: Normal healing progresses through hemostasis (0–2 days) → inflammation (1–4 days) → proliferation (4–21 days) → remodeling (21 days–2 years). Chronic non-healing wounds are arrested in a persistent pro-inflammatory state with elevated matrix metalloproteinases (MMPs), reduced growth factors, and senescent cells, as reviewed in PMC Wound Repair Review (2022).
7. Medication Impact / Treatment
Pharmacologic management is etiology-dependent and directly affects code assignment and clinical indicators:
Antiplatelet / Anticoagulant Agents
Aspirin, clopidogrel (Plavix), ticagrelor, rivaroxaban, and warfarin are used in arterial ulcer patients. Presence of anticoagulation may be relevant to bleeding risk documentation for wound procedures. Use Z79.01 (anticoagulant) or Z79.02 (antiplatelet) as secondary codes per FY2026 Guidelines Section I.C.21.c.3.
Insulin / Antidiabetic Agents
In diabetic foot ulcer patients, insulin use (Z79.4) or oral antidiabetic agents (Z79.84) must be coded when applicable. Long-term insulin use is a secondary code only — it does not change E11 to E10 (Type 1 DM).
Wound-Directed Pharmacology
- Topical antimicrobials: Silver sulfadiazine, cadexomer iodine, PHMB — used for infected/critically colonized wounds
- Becaplermin gel (Regranex, PDGF-BB): FDA-approved for diabetic neuropathic lower-extremity ulcers; limited to one tube/course; requires REMS acknowledgment
- Collagenase (Santyl): Enzymatic debridement agent coded under 97602 (non-selective debridement) when applied by a clinician
- Pentoxifylline: Used off-label for arterial insufficiency and venous ulcers; improves RBC deformability
- Cilostazol: PDE-3 inhibitor approved for claudication in PAD; may improve peripheral perfusion around arterial ulcers
- Systemic antibiotics: For confirmed wound infection; organism-specific; document causative organism for ICD-10-CM B95–B97 codes
- Immunosuppressants (PG, vasculitis): Prednisone, cyclosporine, infliximab; relevant for pathergy-based ulcer management; document underlying condition for accurate L88 vs. L97 assignment
When becaplermin gel (Regranex) is documented in the treatment plan, this confirms a diabetic neuropathic lower-extremity ulcer context. Ensure E11.621 is coded as the lead diabetes complication code, and that L97.5xx with appropriate laterality and depth is assigned as an additional code. Becaplermin is reimbursed under HCPCS J0180 or as a compound; verify payer-specific billing rules.
Preview ends here. The full guide continues with FY2026 ICD-10-CM code sets, CPT surgical coding, MS-DRG mapping, reimbursement guidance, CDI query templates, and an audit checklist — all available to CCO Members.
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