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06 January 2025 : Case report  Austria

[In Press] Rare Lacrimal Gland Melanoma: A Case Report and Treatment Insights

Challenging differential diagnosis, Unusual setting of medical care, Rare disease

Reinhard Told ORCID logo1ABCDEF, Ana-Iris Schiefer ORCID logo2BCDEF, Christoph Hoeller ORCID logo3BCDEF, Adrian Reumueller ORCID logo1ABCEF, Judith Kreminger ORCID logo1ABCDEF, Roman Dunavoelgyi ORCID logo1ABCDEF

DOI: 10.12659/AJCR.946361

Am J Case Rep In Press; DOI: 10.12659/AJCR.946361  

Available online: 2025-01-06, In Press, Corrected Proof

Publication in the "In-Press" formula aims at speeding up the public availability of the pending manuscript while waiting for the final publication. The assigned DOI number is active and citable. The availability of the article in the Medline, PubMed and PMC databases as well as Web of Science will be obtained after the final publication according to the journal schedule

Abstract

BACKGROUND
Melanoma is a malignant transformation of melanocytes known for its capacity to metastasize, necessitating early diagnosis and intervention. While over 97% of melanomas are diagnosed with a known primary site, such as the skin, eye, or mucous membranes, rare cases like melanoma of unknown primary (MUP) can present with atypical manifestations, highlighting the need for comprehensive examinations.
CASE REPORT
In January 2023, a 68-year-old woman presented with a 4-week history of swelling and discoloration in her left upper eyelid, revealing a hard, livid mass indicative of malignancy. Surgery and subsequent histopathology confirmed epithelioid cell melanoma in the lacrimal gland. Although no other primary melanoma sites were found, imaging and biopsy in August 2023 identified metastatic spread to her lungs. Despite proton radiotherapy, progression led to thoracoscopic surgery for metastasis resection in September 2023. Further re-evaluation revealed metastases in both lungs, leading to her enrolment in a trial comparing PD-1 (programmed death ligand 1) antibody plus LAG-3 (lymphocyte activation gene 3) antibody with PD-1 monotherapy. Subsequent progression required treatment with ipilimumab and nivolumab, which resulted in near complete regression of the orbital tumor. Unfortunately, she later developed serious complications, including hypophysitis, lung infection, renal failure, and viral meningitis, which ultimately led to her death in April 2024.
CONCLUSIONS
This case report highlights the diagnostic challenge in distinguishing between melanoma of known and unknown primary origins. It emphasizes the importance of thorough histological work-up and heightened suspicion for melanoma of the lacrimal gland, despite its rarity, to ensure prompt diagnosis and treatment due to its metastatic potential.

Keywords: Lacrimal Apparatus; Melanoma; Orbital Neoplasms

In Press

Case report  China

Right Bundle Branch Block on ECG as a Predictor of Sudden Cardiac Arrest Due to Pulmonary Embolism

Am J Case Rep In Press; DOI: 10.12659/AJCR.946074  

Case report  USA

A 20-Year-Old Woman with Metachronous Polyostotic Simple (Unicameral) Bone Cysts in 9 Sites: A Case Report

Am J Case Rep In Press; DOI: 10.12659/AJCR.946165  

Case report  China

Emergency Management of Cut Throat Injury: A Report of 2 Cases

Am J Case Rep In Press; DOI: 10.12659/AJCR.946414  

Case report  Grenada

Extragastrointestinal Stromal Tumor Mimicking Appendicitis: A Case Study

Am J Case Rep In Press; DOI: 10.12659/AJCR.944665  

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923