Evidence map›Paper›PMID 42639509›Full record

ArticleClinical, cosmetic and investigational dermatology2026

Dermatomal Microcycstic Lymphatic Malformation: A Case Report of an Unusual Presentation.

Ghala Alzhrani, Waseem Alhawsawi, Reema Alzaidi, Fadi Ali Alghamdi, Basil Alghamdi, Sara Makhdoum

Abstract readCase Reports
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ghala AlzhraniCollege of Medicine, King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
Waseem AlhawsawiDepartment of Dermatology, Al-Noor Specialist Hospital, Makkah, Saudi Arabia.
Reema AlzaidiDepartment of Dermatology, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.ORCID 0009-0003-6212-317X
Fadi Ali AlghamdiDepartment of Dermatology, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
Basil AlghamdiCollege of Medicine, King Saud bin Abdulaziz University for Health Sciences, Jeddah, Saudi Arabia.
Sara MakhdoumDepartment of Pathology and Medical Laboratories, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Microcystic lymphatic malformation (MLM), previously termed lymphangioma circumscriptum, is a rare congenital lymphatic malformation typically presenting as grouped translucent or hemorrhagic vesicles resembling frog spawn, most often on the axilla, neck, shoulders, and proximal extremities. Dermatomal distribution is exceptionally rare. Case Presentation: A 17-year-old female presented with a long-standing, gradually enlarging lesion of grouped papules and vesicles along the left flank and lateral thigh, distributed in a linear dermatomal pattern (T10-T12) and sharply respecting the midline. Lesions were translucent, skin-colored, erythematous, and hemorrhagic, with a verrucous surface resembling frog spawn. Histopathology showed dilated papillary dermal lymphatic channels containing proteinaceous fluid and red blood cells, with hyperkeratosis, acanthosis, papillomatosis, and focal dermal fibrosis, confirming MLM. Surgical excision was recommended given the deep lymphatic involvement. Conclusion: This case illustrates a rare dermatomal presentation of MLM, likely reflecting somatic mosaicism of mesodermal lymphatic endothelium. Histopathological confirmation is essential to avoid misdiagnosis, and complete surgical excision remains the preferred treatment to minimize recurrence.

Indexed as

dermatomal distributionlymphangioma circumscriptumlymphatic malformationmicrocystic lymphatic malformation

Identifiers

PMID42639509
PMCPMC13502222

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.