Diagnostic usefulness of bronchoalveolar lavage in Hermansky-Pudlak syndrome: a case with double lung cancers.

A 65-year-old man was admitted to our hospital because of dyspnea on exertion. He had oculocutaneous albinism innately and his parents were consanguineous. His chest roentgenogram on admission showed reticulo-nodular infiltrates and cystic changes throughout both lung fields, and 7 cm mass in the left middle field. Cytology of bronchoalveolar lavage fluid (BALF) revealed macrophages containing ceroid. The diagnosis of HPS was made clinically and the tumor was diagnosed as poorly differentiated adenocarcinoma of the lung. He died of respiratory failure. By autopsy, additional well-differentiated adenocarcinoma was detected. Cytology of BALF was useful to confirm ceroid accumulation in the lung.

[1]  Naoki Oiso,et al.  Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1) , 2003, Nature Genetics.

[2]  B. Roe,et al.  Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6 , 2003, Nature Genetics.

[3]  A. Dwyer,et al.  Hermansky-Pudlak syndrome: radiography and CT of the chest compared with pulmonary function tests and genetic studies. , 2002, AJR. American journal of roentgenology.

[4]  Y. Nasuhara,et al.  Expression and alteration of ras and p53 proteins in patients with lung carcinoma accompanied by idiopathic pulmonary fibrosis , 2002, Cancer.

[5]  R. Nazarian,et al.  The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome. , 2002, Seminars in cell & developmental biology.

[6]  B. Roe,et al.  The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. , 2002, Human molecular genetics.

[7]  Wei Li,et al.  Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene , 2002, Nature Genetics.

[8]  J. Bonifacino,et al.  Hemostasis, Thrombosis, and Vascular Biology Materials and Methods Thrombin-stimulated Platelet Secretion , 2022 .

[9]  W. Gahl,et al.  Nonsense Mutations in ADTB3A Cause Complete Deficiency of the β3A Subunit of Adaptor Complex-3 and Severe Hermansky-Pudlak Syndrome Type 2 , 2002, Pediatric Research.

[10]  E. Ikonen,et al.  Genetic defects of intracellular-membrane transport. , 2000, The New England journal of medicine.

[11]  W. Gahl,et al.  Dermatologic manifestations of Hermansky-Pudlak syndrome in patients with and without a 16-base pair duplication in the HPS1 gene. , 1999, Archives of dermatology.

[12]  E. Kuehl,et al.  Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome). , 1998, The New England journal of medicine.

[13]  M. Ramsay Protein trafficking violations , 1996, Nature Genetics.

[14]  K. Chida,et al.  [Pulmonary interstitial pneumonia in association with Hermansky-Pudlak syndrome]. , 1991, Nihon Kyobu Shikkan Gakkai zasshi.

[15]  H. Tojima,et al.  [Two cases of Hermansky-Pudlak syndrome with interstitial pneumonia]. , 1989, Nihon Kyobu Shikkan Gakkai zasshi.

[16]  V. Kolek,et al.  Hermanský-Pudlák syndrome. , 1985, Acta Universitatis Palackianae Olomucensis Facultatis Medicae.

[17]  J. Rankin,et al.  Hermansky-pudlak syndrome and interstitial lung disease: report of a case with lavage findings. , 1984, The American review of respiratory disease.

[18]  S. Garay,et al.  Hermansky-Pudlak syndrome. Pulmonary manifestations of a ceroid storage disorder. , 1979, The American journal of medicine.

[19]  P. Pudlák,et al.  Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies. , 1959, Blood.