Primary hepatic leiomyosarcoma in a 5-month-old female infant

Pei-Shan Tsai1, Ting-Chi Yeh2, Shin-Lin Shih3

  • 1Department of Radiology, Mackay Memorial Hospital, Taipei, Taiwan.

Insights

Primary hepatic leiomyosarcoma, a rare smooth muscle cancer in the liver, typically affects older adults. This report details the youngest known case in a 5-month-old infant, expanding understanding of this rare pediatric cancer.

Area of Science:

  • Oncology
  • Pediatric Pathology
  • Surgical Pathology

Background:

  • Leiomyosarcoma is a malignant mesenchymal neoplasm originating from smooth muscle cells.
  • Primary hepatic leiomyosarcoma (PHL) is exceptionally rare, with a predilection for middle-aged and elderly individuals.
  • The occurrence of PHL in pediatric populations is exceedingly uncommon.

Observation:

  • This report details a rare case of primary hepatic leiomyosarcoma in a 5-month-old female infant.
  • The patient presented with symptoms indicative of a rapidly growing liver mass.
  • Diagnostic imaging and subsequent histopathological examination confirmed the diagnosis.

Findings:

  • The tumor exhibited features consistent with leiomyosarcoma, arising directly from the liver parenchyma.
  • Molecular and immunohistochemical analyses were performed to characterize the neoplasm.
  • The 5-month-old patient represents the youngest documented case of PHL in the English literature.

Implications:

  • This case challenges the typical age demographic for PHL, suggesting a broader spectrum of presentation.
  • Understanding the youngest cases of PHL is crucial for early diagnosis and tailored treatment strategies in infants.
  • Further research into the etiology and specific characteristics of pediatric PHL is warranted to improve patient outcomes.

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