Littoral cell angioma of the spleen in a 70-year-old male patient with myelodysplastic syndrome: a case report

Introduction: Littoral cell angioma (LCA) is a new subtype of vascular tumor, which has been reported infrequently worldwide.It is associated with visceral malignancies and other immunologic conditions.Clinical case: We present a case of a 70-yearold Caucasian male with a 6-year history of myelodysplastic syndrome, which was investigated for splenomegaly and pancytopenia.Radiological and histopathological examinations revealed an LCA and an open splenectomy were performed.The patient had an uneventful post-operative recovery.Conclusion: LCA is a rare tumor, with atypical presentation often associated with other malignancies or immunologic conditions.Diagnosis is challenging, and so far, splenectomy is the gold standard treatment.

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Publication Details

Journal
Cirugía y Cirujanos (English Edition)
Published
2025-02-05
DOI
https://doi.org/10.24875/cirue.m22000802
Primary Topic
Abdominal Trauma and Injuries
Type
article
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article

Littoral cell angioma of the spleen in a 70-year-old male patient with myelodysplastic syndrome: a case report

Efstathios Kotidis, Orestis Ioannidis, Aggeliki Koltsida, Mantzoros Ioannis et al.
Cirugía y Cirujanos (English Edition)
Abdominal Trauma and Injuries
article

Littoral cell angioma of the spleen in a 70-year-old male patient with myelodysplastic syndrome: a case report

Efstathios Kotidis, Orestis Ioannidis, Aggeliki Koltsida, Mantzoros Ioannis, Angelopoulos Stamatios, Symeonidis Savvas, Papadopoulou Stauroula, Malliora Anastasia, Christidis Panagiotis, Ouzounidis Nikolaos, Pramateftakis Manousos George
article en

Abstract

Introduction: Littoral cell angioma (LCA) is a new subtype of vascular tumor, which has been reported infrequently worldwide.It is associated with visceral malignancies and other immunologic conditions.Clinical case: We present a case of a 70-yearold Caucasian male with a 6-year history of myelodysplastic syndrome, which was investigated for splenomegaly and pancytopenia.Radiological and histopathological examinations revealed an LCA and an open splenectomy were performed.The patient had an uneventful post-operative recovery.Conclusion: LCA is a rare tumor, with atypical presentation often associated with other malignancies or immunologic conditions.Diagnosis is challenging, and so far, splenectomy is the gold standard treatment.

Cirugía y Cirujanos (English Edition)Vol. 92(6)
Life below water
Openalex Percentile: Top 96%
Abdominal Trauma and Injuries
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