2026 ICD-10-CM Diagnosis Code L92.8Other granulomatous disorders of the skin and subcutaneous tissue

ICD-10-CM CodesL00–L99L80-L99L92

ICD-10-CM L92.8
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

L92.8 is a billable ICD-10-CM diagnosis code for other granulomatous disorders of the skin and subcutaneous tissue. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 602 through 603. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified skin disorders.

Code Identity

ICD-10-CM Code
L92.8
Billable Status
Yes — Valid for Submission
Code Describes
Other granulomatous disorders of the skin and subcutaneous tissue
Short Description
Oth granulomatous disorders of the skin, subcu
Parent Code
Granulomatous disorders of skin and subcutaneous tissue

Code Classification

ChapterL00–L99Diseases of the skin and subcutaneous tissue
SectionL80-L99Other disorders of the skin and subcutaneous tissue
CategoryL92Granulomatous disorders of skin and subcutaneous tissue
This CodeL92.8Other granulomatous disorders of the skin and subcutaneous tissue

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • AFC - acanthoma fissuratum cutis
  • Childhood granulomatous periorificial dermatitis
  • Crohn's disease of skin
  • Extraintestinal Crohn's
  • Granuloma multiforme
  • Granulomatous slack skin disease
  • Idiopathic sclerosing lipogranuloma
  • Infantile onset panniculitis with uveitis and systemic granulomatosis
  • Infected umbilical granuloma
  • Infective panniculitis
  • Lipid granuloma of skin caused by mineral oil
  • Lipogranuloma
  • Lobular panniculitis
  • Necrobiotic granulomatous skin disorder
  • Nodule of umbilical structure
  • Omphalitis
  • Paraffinoma of skin
  • Penile sclerosing lipogranuloma
  • Penile sclerosing lipogranuloma due to injection of substance
  • Primary sclerosing lipogranuloma
  • Reproductive system complication of procedure
  • Sarcoidal granuloma of skin
  • Sclerosing lipogranuloma
  • Secondary sclerosing lipogranuloma
  • Starch granuloma of skin
  • Subcutaneous lipochagoma
  • Suture granuloma
  • Trypanosomiasis affecting skin
  • Umbilical granuloma

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Disorder(of)
      • skin
        • granulomatous
          • specified NEC
    • Granulomatosis
      • specified NEC
    • Lipogranuloma, sclerosing

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR SKN007
Other specified and unspecified skin disorders
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Umbilical Granuloma

    excessive granulation tissue at the base of the umbilicus after separation.
  • Omphalitis

    inflammation of the umbilical cord stump in newborns.
  • Granulomatous Slack Skin Disease

    a rare variant of mycosis fungoides, characterized by the development of folds of lax skin in the axillae or groins. it has been reported in association with hodgkin lymphoma. morphologically, there is a dense granulomatous dermal atypical lymphocytic infiltrate, often associated with multinucleated giant cells. destruction of elastic tissue is present. most cases have an indolent clinical course.
  • Erdheim-Chester Disease|ECD|Lipogranulomatosis|Polyostotic Sclerosing Histiocytosis

    a very rare, multisystem non-langerhans cell histiocytosis that predominantly affects adults. it is characterized by the proliferation in the tissues of lipid-laden macrophages and the presence of multinucleated giant cells. it results in sclerosis of the long bones and failure of the affected organs. patients may present with bone pain, exophthalmos, ataxia, liver failure, kidney failure, and hypopituitarism.
  • Farber Lipogranulomatosis

    a very rare autosomal recessive metabolic disorder affecting lipid metabolism. it is caused by mutations in the asah1 gene and is characterized by fatty accumulation in the body tissues. patients develop lipogranulomas in the skin and internal organs, edema and pain in the joints and a hoarse voice. it may be associated with intellectual disability.
  • Large Lipogranuloma Assessment|LPGNLMLG|Large Lipogranuloma|Large Lipogranuloma

    an evaluation of the presence or degree of large lipogranuloma in a sample.
  • Lipogranuloma

    an inflammatory lesion comprised of lipoid material.

Patient EducationClinical

Skin Conditions

Your skin is your body's largest organ. It covers the entire outside of your body. There are many ways that your skin protects your body and helps keep you healthy. For example, it:

The full article covers:

  • What does your skin do?
  • What problems and conditions can affect your skin?
  • How can I keep my skin healthy?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert L92.8 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
686.1 Pyogenic granuloma
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About L92.8Overview

Is L92.8 (Granulomatous disorders of skin and subcutaneous tissue) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report other granulomatous disorders of the skin and subcutaneous tissue on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does L92.8 group to?

When other granulomatous disorders of the skin and subcutaneous tissue is the principal diagnosis on an inpatient stay, it groups to MS-DRG 602, 603, with relative weights from 0.8709 to 1.4213 depending on complications. Higher weights mean higher Medicare reimbursement.

What is the ICD-9 equivalent of L92.8?

Under the General Equivalence Mappings, other granulomatous disorders of the skin and subcutaneous tissue converts to ICD-9-CM 686.1 (pyogenic granuloma). The mapping is approximate, so confirm the match fits the documentation.

Footnotes

[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.