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ALK-rearranged, CD34-positive spindle cell neoplasms resembling dermatofibrosarcoma protuberans: a study of seven cases.
Agrawal, Shruti; Ameline, Baptiste; Folpe, Andrew L; Azzato, Elizabeth; Astbury, Caroline; Mentzel, Thomas; Knapp, Calvin; Rütten, Arno; Creytens, David; Sukov, William; Baumhoer, Daniel; Billings, Steven D; Fritchie, Karen J.
Afiliação
  • Agrawal S; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Ameline B; Department of Dermatology, Mayo Clinic, Rochester, MN, USA.
  • Folpe AL; Bone Tumor Reference Center at the Institute for Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
  • Azzato E; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Astbury C; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
  • Mentzel T; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
  • Knapp C; MVZ Dermatopathologie Friedrichshafen/Bodensee Part G, Friedrichshafen, Germany.
  • Rütten A; Department of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, USA.
  • Creytens D; MVZ Dermatopathologie Friedrichshafen/Bodensee Part G, Friedrichshafen, Germany.
  • Sukov W; Department of Pathology, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Baumhoer D; CRIG, Cancer Research Institute Ghent, Ghent University and Ghent University Hospital, Ghent, Belgium.
  • Billings SD; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Fritchie KJ; Bone Tumor Reference Center at the Institute for Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
Histopathology ; 2024 Jun 13.
Article em En | MEDLINE | ID: mdl-38867577
ABSTRACT

AIMS:

The majority of dermatofibrosarcoma protuberans (DFSP) harbour PDGFB or PDGFD rearrangements. We encountered ALK expression/rearrangement in a PDGFB/D-negative CD34-positive spindle cell neoplasm with features similar to DFSP, prompting evaluation of ALK-rearrangements in DFSP and plaque-like CD34-positive dermal fibroma (P-LDF). METHODS AND

RESULTS:

We searched the archives of academic institutions for cases previously coded as DFSP and P-LDF. NGS-naïve or PDGFB-negative DFSP were screened for ALK (clone D5F3) expression by immunohistochemistry. NGS or ALK FISH was performed on ALK-positive cases. Methylome profiling studies were performed and compared with conventional DFSP. One case of "DFSP" and two "P-LDF" with ALK expression were identified from the archives, while four cases were detected prospectively. These seven cases (6F1M; 8 months to 76 years) arose in the dermis of the arm (two), scalp, eyelid, thigh, abdomen, and shoulder and ranged from 0.4 to 4.2 cm. Tumours were composed of spindled cells and displayed a storiform growth pattern. Cytologic atypia was absent, and mitotic figures were scarce (0-2/10 HPFs, high power fields). The lesional cells were diffusely positive for CD34 and ALK and negative for S100 protein. By NGS (n = 5), ALK fusion partners included DCTN1 (2), PLEKHH2, and CLIP2 in DFSP-like cases and FLNA in P-LDF-like lesions. ALK FISH was positive in one (of two) cases previously labelled P-LDF. Methylome profiling of two (of three) ALK-rearranged DFSP-like tumours showed clustering with conventional DFSP in the UMAP dimension reduction plot. To date, no tumour has recurred (n = 2; 26, 27 months).

CONCLUSION:

We describe a cohort of novel ALK-rearranged tumours with morphologic features similar to DFSP.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article