Evidence map›Paper›PMID 40546990›Full record

ArticleClinical, cosmetic and investigational dermatology2025

Facial Fat Necrosis After Autologous Fat Grafting Caused by Cellulitis: A Case Report.

Jiaxu Gu, Jieyi Wang, Zimo Zhu, Bingcheng Lu, Xiaoming Liu, Bo Yu

Abstract readCase Reports
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jiaxu GuDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
Jieyi WangDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
Zimo ZhuDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.ORCID 0009-0000-7502-4734
Bingcheng LuDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
Xiaoming LiuDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.
Bo YuDepartment of Dermatology, Peking University Shenzhen Hospital, Shenzhen, 518036, People's Republic of China.ORCID 0000-0002-5579-6806

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous fat grafting is a widely used soft tissue filling technique for facial rejuvenation, favored for its high biocompatibility and long-lasting effects. However, the long-term risk of infection due to alterations in local tissue structure remains unclear. This article reports a case of perforating cellulitis in the frontotemporal region of a 39-year-old female patient 3 years after multiple autologous fat grafting procedures. The patient, with no significant prior medical history or immune compromise, developed sudden redness and swelling in the right temporal region, which rapidly spread to the forehead and left temporal region, resulting in perforating abscesses and fat liquefaction necrosis at the filling sites. Laboratory tests identified Staphylococcus aureus as the causative pathogen. The patient was successfully treated with intravenous ceftriaxone sodium and surgical drainage, achieving full recovery with no recurrence during a 6-month follow-up. This case highlights that repeated subcutaneous fat grafting may loosen tissue structure, potentially increasing susceptibility to infection spread. It underscores the importance of vigilance for delayed infections in patients with a history of cosmetic procedures, even years post-operation. Clinicians should consider aesthetic fillings as a possible risk factor for cellulitis and prioritize prompt pathogen identification and aggressive treatment. The findings emphasize the need for long-term monitoring and further research into infection mechanisms post-aesthetic surgery to enhance procedural safety.

Indexed as

autologous fat graftingcellulitisfacial cosmetology

Identifiers

PMID40546990
PMCPMC12182099

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