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Lymphomatoid granulomatosis: A case series from South India.
Sigamani, Elanthenral; Chandramohan, Jagan; Nair, Sheila; Chacko, Geeta; Thomas, Meera; Mathew, Leni Grace; Pulimood, Susanne; Manipadam, Marie Therese.
Afiliação
  • Sigamani E; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Chandramohan J; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Nair S; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Chacko G; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Thomas M; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Mathew LG; Department of Pediatric Oncology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Pulimood S; Department of Dermatology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
  • Manipadam MT; Department of Pathology, Christian Medical College Hospital, Vellore, Tamil Nadu, India.
Indian J Pathol Microbiol ; 61(2): 228-232, 2018.
Article em En | MEDLINE | ID: mdl-29676363
ABSTRACT
CONTEXT Lymphomatoid granulomatosis (LYG) is a rare B-lymphoproliferative disorder characterised by an angiocentric and angiodestructive pattern along with Epstein - Barr virus (EBV) association. It is one of the diagnostic challenges in lymphoma pathology. Deregulation of EBV immune surveillance is one of the narrated hypotheses in the literature. Extrapulmonary manifestations are rare with LYG. Morphological grading is done based on the number of EBV-positive B cells, which is useful to strategize treatment protocol.

AIMS:

We report here a series of nine cases of LYG to discuss the clinical, histological, and immunohistochemistry findings. SETTINGS AND

DESIGN:

This is the first case series from India in published literature. SUBJECTS AND

METHODS:

We reviewed cases of LYG diagnosed at our center for the past 11 years (2006-2016). A total of nine cases were included in this study. Histomorphology was studied in conjunction with immunohistochemistry and clinical details. Cases without classical morphology and negative for EBV immunostain were excluded from the study.

RESULTS:

There were nine patients in our study (7 males and 2 female; MF ratio 3.51). The age of these patients ranged from 4 years to 57 years (mean age 30 years). The most common site involved was the lung (4, 44%), followed by the skin (2, 22%), central nervous system (2, 22%) and lymph node (1, 11%). One patient had primary immunodeficiency. Another patient had undergone renal transplant 11 years before the development of the lesion. Angiocentricity and angioinvasion were appreciated in all nine cases (9/9) with necrosis in four cases (44%) and ill-defined histiocytic aggregates in three cases (33%). The histological features were as follows Grade 1(4 cases, 44%), Grade 2(2 cases, 22%), and Grade 3(3 cases, 33%).

CONCLUSION:

LYG is a rare EBV driven angiodestructive disease with predominantly lung involvement as well as isolated extrapulmonary sites as seen in our study. It is often progressive and ultimately fatal in the absence of appropriate treatment. Grading of the lesion helps to initiate the appropriate treatment of choice.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Herpesvirus Humano 4 / Infecções por Vírus Epstein-Barr / Granulomatose Linfomatoide Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País como assunto: Asia Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Herpesvirus Humano 4 / Infecções por Vírus Epstein-Barr / Granulomatose Linfomatoide Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged País como assunto: Asia Idioma: En Ano de publicação: 2018 Tipo de documento: Article