# Targetoid Hemosiderotic Hemangioma With Spontaneous Remission and Recurrence in a Male Patient: A Case Report

**Authors:** Mridul Bhardwaj, Revat J Meshram, Atharv Sardesai, Dev B Goel

PMC · DOI: 10.7759/cureus.67339 · Cureus · 2024-08-20

## TL;DR

A 23-year-old man had a rare skin lesion called targetoid hemosiderotic hemangioma that disappeared and reappeared on its own.

## Contribution

This case report adds to the limited literature on targetoid hemosiderotic hemangioma in male patients.

## Key findings

- The lesion showed a typical target-like appearance with a blue-black center and red ecchymotic ring.
- Dermoscopic findings were sufficient for diagnosis without needing a biopsy.
- The lesion demonstrated spontaneous remission and recurrence, a rare observation in this condition.

## Abstract

Targetoid hemosiderotic hemangioma is a rare, characteristic, benign lymphovascular lesion that usually affects the trunk and lower limbs. It has a diverse clinical appearance. Most affected people are in their 20s. A violaceous solitary papule encircled by a pale, narrow region and an ecchymotic ring peripherally, mimicking a target, is the most prevalent clinical characteristic. In many cases, the reported dermoscopic signs and patterns of hemosiderotic hemangioma have been found to be adequate for establishing a clinical diagnosis. The following is a case of a 23-year-old male presenting with blue-black vascular lesions on the lateral aspect of the right deltoid with a red ecchymotic ring. The 2×1 cm-sized lesion has a history of spontaneous remission and reappearance. Based on dermoscopic findings, a diagnosis of targetoid hemosiderotic hemangioma was made.

## Linked entities

- **Diseases:** targetoid hemosiderotic hemangioma (MONDO:0003258)

## Full-text entities

- **Diseases:** vascular lesions (MESH:D014652), lymphovascular lesion (MESH:D009059), ecchymotic (MESH:D000094623), Hemosiderotic Hemangioma (MESH:D006391)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC11415134/full.md

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Source: https://tomesphere.com/paper/PMC11415134